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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs402710          
refSNP ID: rs402710
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:80/129
Map to Genome Build:36.3
Citation:NHGRI GWAS PubMed
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/T
Ancestral Allele:C
Clinical Association:unknown
HGVS Names
NM_030782.3:c.1532+9G>A
NT_006576.15:g.1310722C>T
Links

SNP Details are organized in the following sections:
Submission Fasta Resource GeneView Map Diversity Validation

  Submitter records for this RefSNP Cluster back to top
The submission ss44605366 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs402710 during BLAST analysis for the current build.

NCBI
Assay ID
Handle|Submitter IDValidation
Status
ss to rs
Orientation
/Strand
Alleles5' Near Seq 30 bp3' Near Seq 30 bpEntry
Date
Update
Date
Build
Added
Molecule
Type
Freq
Warning
Ancestral
Allele
Success
Rate
ss525010SC_JCM|AC026748.3_33174fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca07/12/0010/25/0680Genomicunknown
ss3253649YUSUKE|IMS-JST063734byFreqrev/TA/Gtggtctacctgtaccagcggtggtgagtgcgctgcgtatgctcggccgttgctccgtctc09/05/0110/10/03100Genomicunknown
ss3441833SC_JCM|AC026748.5_32160rev/TA/Gtggtctacctgtaccagcggtggtgagtgcgctgcgtatgctcggccgttgctccgtctc09/24/0110/10/03100Genomicunknown
ss11723816WI_SSAHASNP|chr5.NT_023089.13_1303460fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca07/03/0310/10/03116Genomicunknown
ss22275420SSAHASNP|WGSA-200403-chr5.chr5.NT_023089.13_1303460fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca03/21/0403/21/04121Genomicunknown
ss44605366ABI|hCV1150769byFreqfwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca07/19/0511/03/06126Genomicunknown
ss65728149ILLUMINA|Human1-rs402710fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca10/10/0610/10/06127Genomicunknown
ss66841117ILLUMINA|HumanHap300v1.1_rs402710fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca11/09/0611/09/06127Genomicunknown
ss67313073ILLUMINA|HumanHap550v1.1_rs402710fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca11/14/0611/14/06127Genomicunknown
ss67719122ILLUMINA|HumanHap650Yv1.0_rs402710fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca11/14/0611/14/06127Genomicunknown
ss68923813PERLEGEN|PGP09639921byFreqfwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca01/30/0708/14/07127Genomicunknown
ss70791707ILLUMINA|HumanHap550v3.0__rs402710fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca04/20/0703/30/08130Genomicunknown
ss71369287ILLUMINA|HumanHap650Yv3.0_rs402710fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca04/23/0704/23/07127Genomicunknown
ss75872386ILLUMINA|ILMN_Human_1M_rs402710fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca08/28/0708/29/07129Genomicunknown
ss77444578HGSV|Cor12156_SNV_20070510.chr5_1373722fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca10/09/0710/13/07129Genomicunknown
ss79174029ILLUMINA|HumanHap300v2.0_rs402710fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca04/18/0711/18/07130Genomicunknown
ss83425426HGSV|Cor19240_SNV_20070510.chr5_1373722fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca11/30/0712/05/07130Genomicunknown
ss83447001KRIBB_YJKIM|KHS463780fwd/BC/Tgagacggagcaacggccgagcatacgcagcgcactcaccaccgctggtacaggtagacca12/04/0712/05/07130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs402710|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=130
 TGACTGTGAA TAGGTAAATA AATCGCTTAA GGAGAGACAT TTGCTTTCAG TGGCTCATCA
 ATAATTCACA TAGAAACGAG CATTTCTAAA GCACAGTGAG GAGACAGAGC TGGAACAGTT
 TCTTGCCAGG ACATATCATG GGCAACTGGA ACCCAAGTTT AGGCAAGACA GGAAAAACCA
 CCACCTGCAA ATTATCTTTT CCCTCAAATG GATAAACAGG CGCAGGGTGC GGTGAAAGCC
 GTCATTCCGT TCAGCAGCAG CCACGCCGCT GAGACGGAGC AACGGCCGAG CATACGCAGC
 Y
 GCACTCACCA CCGCTGGTAC AGGTAGACCA GAAACACCAC GTCGTCCCGG AAGCAGGCCA
 GCCGGTGAGA CGTGGGCATG GTGATGATGA AGGCAAAGAC GTCATCAATG AAGGTGTTGA
 AAGCCTGCAG GGCCAGACGG GAGGAGGGTG AACCCCAGTT GCTGGGGCTG GAATCCTACT
 GTTTTTGGTA ACCTAACCAA GCCAACGGCT TTTGGCAGAT GCTTGGAACT AACTGGAACT
 CCTCACAGCA ACAACAAAAA GAGCAGAAAG CCGGCAAGTG GAGATACGGA GCTCTGTTCC

  GeneView back to top
GeneView via analysis of contig annotation: CLPTM1L CLPTM1-like
View variations for gene:
Include clinically associated: in gene region cSNP has frequency double hit
Group
Label
Contig->mRNAGene Model (contig mRNA transcript) Color Legend
referenceNT_006576->NM_030782
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_006576->NM_030782->NP_1104091310722reverseintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs402710 maps exactly once on NCBI human chromosome 5
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
5NW_001838923.28219561301015minusAalt_assembly_8HuRefHuRefview300
5NW_922518.14600101357578plusTalt_assembly_1CeleraCeleraview300
5NT_006576.1513107221373722plusCref_assemblyreferencereferenceview300

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_023089 AC022130
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank mRNA:
CT824641.5 AK126225.1
UniGene Cluster ID
444673

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceC/C
C/T
T/T
HWPC
T
ss3253649JBIC-allele 1484AF 0.679 0.321
ss44605366HapMap-CEUEuropean 116IG 0.431 0.483 0.086 0.317 0.672 0.328
HapMap-HCBAsian 90IG 0.556 0.356 0.089 0.584 0.733 0.267
HapMap-JPTAsian 88IG 0.409 0.523 0.068 0.251 0.670 0.330
HapMap-YRISub-Saharan African 118IG 0.220 0.559 0.220 0.317 0.500 0.500
AoD_African_American 90AF 0.540 0.460
AoD_Caucasian 92AF 0.640 0.360
ss68923813HapMap-CEUEuropean 120GF 0.450 0.550 0.725 0.275
HapMap-HCBAsian 90GF 0.756 0.244 0.878 0.122
HapMap-JPTAsian 90GF 0.556 0.444 0.778 0.222
HapMap-YRISub-Saharan African 120GF 0.333 0.667 0.667 0.333
Concordant GenotypeTotal SampleC/CC/TT/T
ss446053661999994
ss6892381319910198
RefSNP Genotype SummaryTotal IndividualC/CC/TT/T
rs40271027010198
Discordant Genotypes:
Indiviudal
SampleID
SubSNP(ss)GenotypePopulation
Handle
Submitter
Population
Submitter
SampleID
SampleID
Alias
Submission
Batch
NCBI
ProbeID
157ss44605366C/TCSHL-HAPMAPHapMap-CEUNA12144CEPH1334.10r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
157ss68923813C/CCSHL-HAPMAPHapMap-CEUNA12144CEPH1334.10chr5-HapMap-CEU
159ss44605366T/TCSHL-HAPMAPHapMap-CEUNA12146CEPH1334.12r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
159ss68923813C/TCSHL-HAPMAPHapMap-CEUNA12146CEPH1334.12chr5-HapMap-CEU
174ss44605366T/TCSHL-HAPMAPHapMap-CEUNA07048CEPH1341.01r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
174ss68923813C/TCSHL-HAPMAPHapMap-CEUNA07048CEPH1341.01chr5-HapMap-CEU
175ss44605366T/TCSHL-HAPMAPHapMap-CEUNA06991CEPH1341.02r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
175ss68923813C/TCSHL-HAPMAPHapMap-CEUNA06991CEPH1341.02chr5-HapMap-CEU
185ss44605366T/TCSHL-HAPMAPHapMap-CEUNA07055CEPH1341.12r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
185ss68923813C/TCSHL-HAPMAPHapMap-CEUNA07055CEPH1341.12chr5-HapMap-CEU
242ss44605366T/TCSHL-HAPMAPHapMap-CEUNA10854CEPH1349.02r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
242ss68923813C/TCSHL-HAPMAPHapMap-CEUNA10854CEPH1349.02chr5-HapMap-CEU
348ss44605366T/TCSHL-HAPMAPHapMap-CEUNA10860CEPH1362.01r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
348ss68923813C/TCSHL-HAPMAPHapMap-CEUNA10860CEPH1362.01chr5-HapMap-CEU
366ss44605366C/TCSHL-HAPMAPHapMap-CEUNA10863CEPH1375.02r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
366ss68923813C/CCSHL-HAPMAPHapMap-CEUNA10863CEPH1375.02chr5-HapMap-CEU
373ss44605366T/TCSHL-HAPMAPHapMap-CEUNA12264CEPH1375.11r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
373ss68923813C/TCSHL-HAPMAPHapMap-CEUNA12264CEPH1375.11chr5-HapMap-CEU
410ss44605366T/TCSHL-HAPMAPHapMap-CEUNA12155CEPH1408.12r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
410ss68923813C/TCSHL-HAPMAPHapMap-CEUNA12155CEPH1408.12chr5-HapMap-CEU
429ss44605366C/TCSHL-HAPMAPHapMap-CEUNA10835CEPH1416.01r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
429ss68923813C/CCSHL-HAPMAPHapMap-CEUNA10835CEPH1416.01chr5-HapMap-CEU
537ss44605366T/TCSHL-HAPMAPHapMap-CEUNA12752CEPH1447.01r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
537ss68923813C/TCSHL-HAPMAPHapMap-CEUNA12752CEPH1447.01chr5-HapMap-CEU
579ss44605366T/TCSHL-HAPMAPHapMap-CEUNA12815CEPH1454.15r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
579ss68923813C/TCSHL-HAPMAPHapMap-CEUNA12815CEPH1454.15chr5-HapMap-CEU
610ss44605366C/TCSHL-HAPMAPHapMap-CEUNA12864CEPH1459.01r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
610ss68923813C/CCSHL-HAPMAPHapMap-CEUNA12864CEPH1459.01chr5-HapMap-CEU
618ss44605366C/TCSHL-HAPMAPHapMap-CEUNA12872CEPH1459.09r23_ch5_CEU_illumina:infinium_genotyping_1.0.0
618ss68923813C/CCSHL-HAPMAPHapMap-CEUNA12872CEPH1459.09chr5-HapMap-CEU
5133ss44605366T/TCSHL-HAPMAPHapMap-YRINA18502YOR004.02r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5133ss68923813C/TCSHL-HAPMAPHapMap-YRINA18502YOR004.02chr5-HapMap-YRI
5135ss44605366C/TCSHL-HAPMAPHapMap-YRINA19128YOR077.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5135ss68923813C/CCSHL-HAPMAPHapMap-YRINA19128YOR077.03chr5-HapMap-YRI
5139ss44605366C/TCSHL-HAPMAPHapMap-YRINA19100YOR105.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5139ss68923813C/CCSHL-HAPMAPHapMap-YRINA19100YOR105.01chr5-HapMap-YRI
5144ss44605366C/TCSHL-HAPMAPHapMap-YRINA19192YOR112.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5144ss68923813C/CCSHL-HAPMAPHapMap-YRINA19192YOR112.03chr5-HapMap-YRI
5149ss44605366T/TCSHL-HAPMAPHapMap-HCBNA18524CH18524r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5149ss68923813C/TCSHL-HAPMAPHapMap-HCBNA18524CH18524chr5-HapMap-HCB
5151ss44605366C/TCSHL-HAPMAPHapMap-HCBNA18558CH18558r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5151ss68923813C/CCSHL-HAPMAPHapMap-HCBNA18558CH18558chr5-HapMap-HCB
5156ss44605366C/TCSHL-HAPMAPHapMap-HCBNA18603CH18603r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5156ss68923813C/CCSHL-HAPMAPHapMap-HCBNA18603CH18603chr5-HapMap-HCB
5157ss44605366T/TCSHL-HAPMAPHapMap-HCBNA18540CH18540r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5157ss68923813C/TCSHL-HAPMAPHapMap-HCBNA18540CH18540chr5-HapMap-HCB
5158ss44605366C/TCSHL-HAPMAPHapMap-HCBNA18605CH18605r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5158ss68923813C/CCSHL-HAPMAPHapMap-HCBNA18605CH18605chr5-HapMap-HCB
5169ss44605366C/TCSHL-HAPMAPHapMap-HCBNA18564CH18564r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5169ss68923813C/CCSHL-HAPMAPHapMap-HCBNA18564CH18564chr5-HapMap-HCB
5171ss44605366C/TCSHL-HAPMAPHapMap-HCBNA18563CH18563r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5171ss68923813C/CCSHL-HAPMAPHapMap-HCBNA18563CH18563chr5-HapMap-HCB
5174ss44605366C/TCSHL-HAPMAPHapMap-HCBNA18571CH18571r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5174ss68923813C/CCSHL-HAPMAPHapMap-HCBNA18571CH18571chr5-HapMap-HCB
5180ss44605366C/TCSHL-HAPMAPHapMap-HCBNA18623CH18623r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5180ss68923813C/CCSHL-HAPMAPHapMap-HCBNA18623CH18623chr5-HapMap-HCB
5182ss44605366T/TCSHL-HAPMAPHapMap-HCBNA18577CH18577r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5182ss68923813C/TCSHL-HAPMAPHapMap-HCBNA18577CH18577chr5-HapMap-HCB
5189ss44605366T/TCSHL-HAPMAPHapMap-HCBNA18592CH18592r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5189ss68923813C/TCSHL-HAPMAPHapMap-HCBNA18592CH18592chr5-HapMap-HCB
5191ss44605366C/TCSHL-HAPMAPHapMap-HCBNA18593CH18593r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5191ss68923813C/CCSHL-HAPMAPHapMap-HCBNA18593CH18593chr5-HapMap-HCB
5192ss44605366C/TCSHL-HAPMAPHapMap-HCBNA18637CH18637r23_ch5_HCB_illumina:infinium_genotyping_1.0.0
5192ss68923813C/CCSHL-HAPMAPHapMap-HCBNA18637CH18637chr5-HapMap-HCB
5199ss44605366C/TCSHL-HAPMAPHapMap-JPTNA18945JA18945r23_ch5_JPT_illumina:infinium_genotyping_1.0.0
5199ss68923813C/CCSHL-HAPMAPHapMap-JPTNA18945JA18945chr5-HapMap-JPT
5201ss44605366C/TCSHL-HAPMAPHapMap-JPTNA18948JA18948r23_ch5_JPT_illumina:infinium_genotyping_1.0.0
5201ss68923813C/CCSHL-HAPMAPHapMap-JPTNA18948JA18948chr5-HapMap-JPT
5204ss44605366C/TCSHL-HAPMAPHapMap-JPTNA18964JA18964r23_ch5_JPT_illumina:infinium_genotyping_1.0.0
5204ss68923813C/CCSHL-HAPMAPHapMap-JPTNA18964JA18964chr5-HapMap-JPT
5210ss44605366T/TCSHL-HAPMAPHapMap-JPTNA18961JA18961r23_ch5_JPT_illumina:infinium_genotyping_1.0.0
5210ss68923813C/TCSHL-HAPMAPHapMap-JPTNA18961JA18961chr5-HapMap-JPT
5217ss44605366C/TCSHL-HAPMAPHapMap-JPTNA18976JA18976r23_ch5_JPT_illumina:infinium_genotyping_1.0.0
5217ss68923813C/CCSHL-HAPMAPHapMap-JPTNA18976JA18976chr5-HapMap-JPT
5218ss44605366T/TCSHL-HAPMAPHapMap-JPTNA18978JA18978r23_ch5_JPT_illumina:infinium_genotyping_1.0.0
5218ss68923813C/TCSHL-HAPMAPHapMap-JPTNA18978JA18978chr5-HapMap-JPT
5223ss44605366C/TCSHL-HAPMAPHapMap-JPTNA18971JA18971r23_ch5_JPT_illumina:infinium_genotyping_1.0.0
5223ss68923813C/CCSHL-HAPMAPHapMap-JPTNA18971JA18971chr5-HapMap-JPT
5229ss44605366T/TCSHL-HAPMAPHapMap-JPTNA18992JA18992r23_ch5_JPT_illumina:infinium_genotyping_1.0.0
5229ss68923813C/TCSHL-HAPMAPHapMap-JPTNA18992JA18992chr5-HapMap-JPT
5232ss44605366C/TCSHL-HAPMAPHapMap-JPTNA19000JA19000r23_ch5_JPT_illumina:infinium_genotyping_1.0.0
5232ss68923813C/CCSHL-HAPMAPHapMap-JPTNA19000JA19000chr5-HapMap-JPT
5240ss44605366T/TCSHL-HAPMAPHapMap-YRINA18504YOR005.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5240ss68923813C/TCSHL-HAPMAPHapMap-YRINA18504YOR005.03chr5-HapMap-YRI
5243ss44605366T/TCSHL-HAPMAPHapMap-YRINA18507YOR009.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5243ss68923813C/TCSHL-HAPMAPHapMap-YRINA18507YOR009.03chr5-HapMap-YRI
5244ss44605366C/TCSHL-HAPMAPHapMap-YRINA18860YOR012.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5244ss68923813C/CCSHL-HAPMAPHapMap-YRINA18860YOR012.01chr5-HapMap-YRI
5247ss44605366T/TCSHL-HAPMAPHapMap-YRINA18515YOR013.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5247ss68923813C/TCSHL-HAPMAPHapMap-YRINA18515YOR013.01chr5-HapMap-YRI
5248ss44605366T/TCSHL-HAPMAPHapMap-YRINA18517YOR013.02r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5248ss68923813C/TCSHL-HAPMAPHapMap-YRINA18517YOR013.02chr5-HapMap-YRI
5249ss44605366T/TCSHL-HAPMAPHapMap-YRINA18516YOR013.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5249ss68923813C/TCSHL-HAPMAPHapMap-YRINA18516YOR013.03chr5-HapMap-YRI
5252ss44605366C/TCSHL-HAPMAPHapMap-YRINA18522YOR016.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5252ss68923813C/CCSHL-HAPMAPHapMap-YRINA18522YOR016.03chr5-HapMap-YRI
5253ss44605366T/TCSHL-HAPMAPHapMap-YRINA18872YOR017.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5253ss68923813C/TCSHL-HAPMAPHapMap-YRINA18872YOR017.01chr5-HapMap-YRI
5256ss44605366C/TCSHL-HAPMAPHapMap-YRINA18854YOR018.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5256ss68923813C/CCSHL-HAPMAPHapMap-YRINA18854YOR018.01chr5-HapMap-YRI
5257ss44605366T/TCSHL-HAPMAPHapMap-YRINA18852YOR018.02r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5257ss68923813C/TCSHL-HAPMAPHapMap-YRINA18852YOR018.02chr5-HapMap-YRI
5265ss44605366T/TCSHL-HAPMAPHapMap-YRINA18914YOR028.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5265ss68923813C/TCSHL-HAPMAPHapMap-YRINA18914YOR028.01chr5-HapMap-YRI
5266ss44605366T/TCSHL-HAPMAPHapMap-YRINA18912YOR028.02r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5266ss68923813C/TCSHL-HAPMAPHapMap-YRINA18912YOR028.02chr5-HapMap-YRI
5267ss44605366T/TCSHL-HAPMAPHapMap-YRINA18913YOR028.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5267ss68923813C/TCSHL-HAPMAPHapMap-YRINA18913YOR028.03chr5-HapMap-YRI
5270ss44605366C/TCSHL-HAPMAPHapMap-YRINA19092YOR040.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5270ss68923813C/CCSHL-HAPMAPHapMap-YRINA19092YOR040.03chr5-HapMap-YRI
5271ss44605366T/TCSHL-HAPMAPHapMap-YRINA19103YOR042.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5271ss68923813C/TCSHL-HAPMAPHapMap-YRINA19103YOR042.01chr5-HapMap-YRI
5272ss44605366C/TCSHL-HAPMAPHapMap-YRINA19102YOR042.02r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5272ss68923813C/CCSHL-HAPMAPHapMap-YRINA19102YOR042.02chr5-HapMap-YRI
5277ss44605366T/TCSHL-HAPMAPHapMap-YRINA19202YOR045.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5277ss68923813C/TCSHL-HAPMAPHapMap-YRINA19202YOR045.01chr5-HapMap-YRI
5279ss44605366T/TCSHL-HAPMAPHapMap-YRINA19200YOR045.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5279ss68923813C/TCSHL-HAPMAPHapMap-YRINA19200YOR045.03chr5-HapMap-YRI
5282ss44605366T/TCSHL-HAPMAPHapMap-YRINA19171YOR047.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5282ss68923813C/TCSHL-HAPMAPHapMap-YRINA19171YOR047.03chr5-HapMap-YRI
5283ss44605366C/TCSHL-HAPMAPHapMap-YRINA19205YOR048.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5283ss68923813C/CCSHL-HAPMAPHapMap-YRINA19205YOR048.01chr5-HapMap-YRI
5284ss44605366C/TCSHL-HAPMAPHapMap-YRINA19204YOR048.02r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5284ss68923813C/CCSHL-HAPMAPHapMap-YRINA19204YOR048.02chr5-HapMap-YRI
5285ss44605366T/TCSHL-HAPMAPHapMap-YRINA19203YOR048.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5285ss68923813C/TCSHL-HAPMAPHapMap-YRINA19203YOR048.03chr5-HapMap-YRI
5286ss44605366T/TCSHL-HAPMAPHapMap-YRINA19211YOR050.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5286ss68923813C/TCSHL-HAPMAPHapMap-YRINA19211YOR050.01chr5-HapMap-YRI
5288ss44605366T/TCSHL-HAPMAPHapMap-YRINA19210YOR050.03r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5288ss68923813C/TCSHL-HAPMAPHapMap-YRINA19210YOR050.03chr5-HapMap-YRI
5295ss44605366T/TCSHL-HAPMAPHapMap-YRINA19221YOR058.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5295ss68923813C/TCSHL-HAPMAPHapMap-YRINA19221YOR058.01chr5-HapMap-YRI
5298ss44605366C/TCSHL-HAPMAPHapMap-YRINA19120YOR060.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5298ss68923813C/CCSHL-HAPMAPHapMap-YRINA19120YOR060.01chr5-HapMap-YRI
5299ss44605366C/TCSHL-HAPMAPHapMap-YRINA19116YOR060.02r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5299ss68923813C/CCSHL-HAPMAPHapMap-YRINA19116YOR060.02chr5-HapMap-YRI
5304ss44605366T/TCSHL-HAPMAPHapMap-YRINA19154YOR072.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5304ss68923813C/TCSHL-HAPMAPHapMap-YRINA19154YOR072.01chr5-HapMap-YRI
5307ss44605366T/TCSHL-HAPMAPHapMap-YRINA19145YOR074.01r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5307ss68923813C/TCSHL-HAPMAPHapMap-YRINA19145YOR074.01chr5-HapMap-YRI
5308ss44605366T/TCSHL-HAPMAPHapMap-YRINA19143YOR074.02r23_ch5_YRI_illumina:infinium_genotyping_1.0.0
5308ss68923813C/TCSHL-HAPMAPHapMap-YRINA19143YOR074.02chr5-HapMap-YRI
Genotype data submitted for270 samples from270 individualsIndividual with multiple genotypes submission:270

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqwith2hitwithHapMapFreq
DoubleHit found by:  BCM_SSAHASNPNCBI
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .