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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs2822628          
refSNP ID: rs2822628
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:100/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/G
Ancestral Allele:G
Clinical Association:unknown
HGVS Names
Links , Linkout

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 ss44246726 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs2822628 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
ss3997069PERLEGEN|P00201574byFreqfwd/TC/Gtgtgatcagagaccccagaaaagtgagctaatccctgtaatggcctgcgtggcaagactc09/26/0104/07/04100Genomicunknown
ss24225982PERLEGEN|afd0004743byFreqfwd/TC/Gtgtgatcagagaccccagaaaagtgagctaatccctgtaatggcctgcgtggcaagactc08/10/0409/13/04123Genomicunknown
ss44246726ABI|hCV16123694byFreqfwd/C/Gtgtgatcagagaccccagaaaagtgagctaatccctgtaatggcctgcgtggcaagactc07/18/0511/03/06126Genomicunknown
ss76480284AFFY|AFFY_6_1M_SNP_A-8341102fwd/C/Gccagaaaagtgagctaatccctgtaatggcct08/28/0708/30/07129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs2822628|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/G'|mol=Genomic|build=129
 ACAGCTCCTG AGCCACCAGG GCCTGTTTAA AGTACACCAT GGCCGATTCT TTCTAGGGAA
 GAGGAAGGAA AAGTAAATTG GTAGCTCTAG GCTGGGAAAC CACTGACTAA GAGAAAGGAA
 AGAAAAAAAA AGAGCAATGC CCTATGAAAA GTCACTATTT AATTGAATCT TCTTTTGTCA
 AGACTACTAC TCTAAAAGCC TTGTTCCTAA AAAATGTAAG GGGCTACTTT GCCTTCACCA
 TTGTTTGTTG CCTTACGATA GCCCACTTCA TGTGATCAGA GACCCCAGAA AAGTGAGCTA
 S
 ATCCCTGTAA TGGCCTGCGT GGCAAGACTC CCACCACCCC TTCTTTGATC ACTTTCTCCC
 TACCCCTCTG TGTTTCTGCG ACATTGGCCT CCATGCTGTG TCATGAGTTT GCCAGGCCAA
 TTCACGCCTA CCACAGGGAT TTTACATCTG CTATTTCCTT TACCTGGAAC AAGTTTTTAC
 TGGAAATCTG TAAGCCTCAC TCTCCATGTC CTTCAGTTCT TGCCTTAAAA TTCTCCAGAG
 GATTTCTTTG GCACACCCAT CTAACATGCC CATCCCACAT CTACACTTTA TACCCCACTT

  GeneView back to top
GeneView: no link established by analysis of contig annotation
GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs2822628 maps exactly once on NCBI human chromosome 21
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
21NW_927384.1376068890945plusGalt_assembly_1CeleraCeleraview300
21NW_001838706.15334821104068plusCalt_assembly_8HuRefHuRefview300
21NT_011512.10139557514655575plusGref_assemblyreferencereferenceview300

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_002836
dbSNP Blast Analysis
GenBank HTGS Finished:
AF130249.1 AF130358.2

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceC/C
C/G
G/G
HWPC
G
ss24225982AFD_EUR_PANELEuropean 48IG 0.083 0.542 0.375 0.371 0.354 0.646
AFD_AFR_PANELAfrican American 46IG 0.043 0.261 0.696 0.752 0.174 0.826
AFD_CHN_PANELAsian 48IG 0.083 0.583 0.333 0.251 0.375 0.625
ss3997069NCBI|NIHPDR 18AF 0.278 0.722
ss44246726HapMap-CEUEuropean 120IG 0.117 0.400 0.483 0.584 0.317 0.683
HapMap-HCBAsian 90IG 0.111 0.556 0.333 0.273 0.389 0.611
HapMap-JPTAsian 88IG 0.114 0.409 0.477 0.752 0.318 0.682
HapMap-YRISub-Saharan African 120IG 0.050 0.383 0.567 0.752 0.242 0.758

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.427+/-0.17733226090

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqbySubmitterwithHapMapFreq
Validated by: PERLEGEN
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .