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BUILD 130
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Reference SNP(refSNP) Cluster Report: rs2305962          
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:100/130
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/G
Ancestral Allele:C
Clinical Association:unknown
HGVS Names
NT_006713.14:g.14585831G>C
XM_001720146.1:c.331C>G
XM_001720158.1:c.331G>C
XM_001722781.1:c.331C>G
XP_001720198.1:p.Pro111Ala
XP_001720210.1:p.Ala111Pro
XP_001722833.1:p.Pro111Ala
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 ss44658305 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs2305962 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
ss3253343YUSUKE|IMS-JST063428fwd/TC/Ggatactgattaccttcttgagtggaagaagctctaagtgttgaagcttaaggccagtgtc09/05/0110/10/03100Genomicunknown
ss14684175WI_SSAHASNP|chr5.NT_006431.13_14556215byFreqrev/BC/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc11/05/0310/25/06119Genomicunknown
ss22366629SSAHASNP|WGSA-200403-chr5.chr5.NT_006431.13_14556215rev/BC/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc03/21/0403/21/04121Genomicunknown
ss23895733PERLEGEN|afd3287299byFreqrev/BC/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc08/10/0409/13/04123Genomicunknown
ss44658305ABI|hCV3076493byFreqrev/C/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc07/19/0511/03/06126Genomicunknown
ss68936958PERLEGEN|PGP03287299byFreqrev/C/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc01/30/0708/14/07127Genomicunknown
ss74809889AFFY|SNP_M-183153fwd/TC/Ggatactgattaccttcttgagtggaagaagctctaagtgttgaagcttaaggccagtgtc08/09/0708/09/07128Genomicunknown
ss74878442ILLUMINA|ILMN_Human_1M_rs2305962fwd/C/Ggatactgattaccttcttgagtggaagaagctctaagtgttgaagcttaaggccagtgtc08/28/0708/29/07129Genomicunknown
ss80007929HGSV|Cor18507_SNV_20070510.chr5_64027229rev/C/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc11/23/0711/24/07130Genomicunknown
ss83147981HGSV|Cor18555_SNV_20070510.chr5_64027229rev/C/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc11/27/0712/04/07130Genomicunknown
ss93120114BCMHGSC_JDW|JWB-1986916rev/C/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc02/26/0803/03/08129Genomicunknown
ss98622690HUMANGENOME_JCVI|1103654119830rev/C/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc04/01/0804/01/08130Genomicunknown
ss1090906341000GENOMES|CEU.trio.12.15.2008_1277943_chr5_64027229rev/C/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc12/15/0812/16/08130Genomicunknown
ss116641780ILLUMINA-UK|NA18507_000082708_NCBI36.1_chr5_64027229rev/C/Ggacactggccttaagcttcaacacttagagcttcttccactcaagaaggtaatcagtatc01/17/0901/17/09130Genomic99 %

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs2305962|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/G'|mol=Genomic|build=130
 TTTAATAACT GGAAGGAACA TAAATATATT TAAAGCAGAT TTACTGAACC AATGATTTAA
 TTTTCATGAG AATAATTACA TCCTGCTGCT ATTTTTCCTT CAGCACAATT TCCCTAAGGT
 ATTTCATCAT TAACGGCCTG ATTCAATGTG AATTTTTAGT GAGACACATA GTGAACTGAA
 TTTTTAAAAA GCATTCATTG TTAACAGTAT TATCACCCAG GTACAAGTTA TTCTTTTGGA
 TAGAGTTCAG GTAATTGGTA ACAAATAATA GATACTGATT ACCTTCTTGA GTGGAAGAAG
 S
 CTCTAAGTGT TGAAGCTTAA GGCCAGTGTC TAATCTTTGA GGTTTCGTAT ACAGAAATAA
 ATAGCAAAGG ACACAGACAC TGATGACAAA GGCGAGTAAA ACAAGGGCAG CAATTCCTAG
 TCCAATCAAG GCACCAATGC TGAGGAAAAC AGAAAAAAAA TATGTGTCAC ACAAAGTGGT
 TCACACTGGT TCAACTAAAG AGAAGGCATA AATATATTGT TAATTCTTGT TTTCAGTTAT
 TCATAACCAA ATTGTATTTT AGCATAAAAA GGAACTGATT GAAATCTACA GTTCACCTTT

  GeneView back to top

GeneView via analysis of contig annotation:  

View more variation on this gene (click to hide).
Include clinically associated: in gene region cSNP has frequency double hit
Assembly SNP to Chr Chr Chr position Contig Contig position Allele
Function mRNA Protein
mRNA to Chr Accession Position Allele change Accession Position Residue change
on assembly: is labeled at position on chromosome .

GeneView via analysis of contig annotation: N/A.

GeneView via direct blast against RefSeq sequences (used when no gene model is available):

Function Chr mRNA Protein
SNP to mRNA Accession Position Allele change Accession Position Residue change
on assembly: is labeled at position on chromosome .

GeneView via direct blast against RefSeq sequences (used when no gene model is available): N/A


  Integrated Maps: back to top
Genome Build Chr Chr Pos Contig Contig Pos SNP to
Chr
Contig
allele
Group term Group label Contig label Neighbor
SNP
Map Method
doesn't map to any assembly.

  NCBI Resource Links back to top
Resource
Submitter-Referenced
GenBank
NT_006431 ABBA01048338
dbSNP Blast Analysis
UniGene Cluster ID
69504

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss# Population Individual
Group
Chrom.
Sample Cnt.
Source C/C
C/G
G/G
HWP C
G
N
ss14684175 CHMJ Asian 74 IG 0.459 0.514 0.027
ss23895733 AFD_EUR_PANEL European 48 IG 0.583 0.333 0.083 0.655 0.750 0.250
AFD_AFR_PANEL African American 46 IG 0.304 0.522 0.174 1.000 0.565 0.435
AFD_CHN_PANEL Asian 48 IG 0.125 0.625 0.250 0.200 0.438 0.562
ss44658305 HapMap-CEU European 120 IG 0.483 0.367 0.150 0.200 0.667 0.333
HapMap-HCB Asian 90 IG 0.200 0.578 0.222 0.317 0.489 0.511
HapMap-JPT Asian 88 IG 0.227 0.432 0.341 0.439 0.443 0.557
HapMap-YRI Sub-Saharan African 118 IG 0.441 0.458 0.102 1.000 0.669 0.331
AoD_African_American 90 AF 0.580 0.420
AoD_Caucasian 92 AF 0.700 0.300
ss68936958 HapMap-CEU European 120 GF 1.000 0.500 0.500
HapMap-HCB Asian 90 GF 1.000 0.500 0.500
HapMap-JPT Asian 90 GF 1.000 0.500 0.500
HapMap-YRI Sub-Saharan African 120 GF 1.000 0.500 0.500
Concordant Genotype Total Sample C/C C/G G/G
ss23895733 64 12 35 17
ss44658305 374 117
ss98622690 1 1
RefSNP Genotype Summary Total Individual C/C C/G G/G
rs2305962 582 13 150 17
Discordant Genotypes:
Indiviudal
SampleID
SubSNP(ss) Genotype Population
Handle
Submitter
Population
Submitter
SampleID
SampleID
Alias
Submission
Batch
NCBI
ProbeID
150 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA10846 CEPH1334.01 r27_ch5_CEU_bcm:genotype_0002
157 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12144 CEPH1334.10 r27_ch5_CEU_bcm:genotype_0002
158 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12145 CEPH1334.11 r27_ch5_CEU_bcm:genotype_0002
162 ss23895733 G/G PERLEGEN AFD_EUR_PANEL NA07019 71_IND_CHR_5
162 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA07019 CEPH1340.02 r27_ch5_CEU_bcm:genotype_0002
169 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA06994 CEPH1340.09 r27_ch5_CEU_bcm:genotype_0002
170 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA07000 CEPH1340.10 r27_ch5_CEU_bcm:genotype_0002
171 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA07022 CEPH1340.11 r27_ch5_CEU_bcm:genotype_0002
174 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA07048 CEPH1341.01 r27_ch5_CEU_bcm:genotype_0002
175 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA06991 CEPH1341.02 r27_ch5_CEU_bcm:genotype_0002
184 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA07034 CEPH1341.11 r27_ch5_CEU_bcm:genotype_0002
185 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA07055 CEPH1341.12 r27_ch5_CEU_bcm:genotype_0002
186 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA06993 CEPH1341.13 r27_ch5_CEU_bcm:genotype_0002
187 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA06985 CEPH1341.14 r27_ch5_CEU_bcm:genotype_0002
188 ss23895733 G/G PERLEGEN AFD_EUR_PANEL NA10851 71_IND_CHR_5
188 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA10851 CEPH1344.01 r27_ch5_CEU_bcm:genotype_0002
200 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12057 CEPH1344.13 r27_ch5_CEU_bcm:genotype_0002
203 ss23895733 G/G PERLEGEN AFD_EUR_PANEL NA07348 71_IND_CHR_5
203 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA07348 CEPH1345.02 r27_ch5_CEU_bcm:genotype_0002
213 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA07357 CEPH1345.12 r27_ch5_CEU_bcm:genotype_0002
215 ss23895733 G/G PERLEGEN AFD_EUR_PANEL NA10857 71_IND_CHR_5
215 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA10857 CEPH1346.01 r27_ch5_CEU_bcm:genotype_0002
225 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12043 CEPH1346.11 r27_ch5_CEU_bcm:genotype_0002
226 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12044 CEPH1346.12 r27_ch5_CEU_bcm:genotype_0002
229 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA10859 CEPH1347.02 r27_ch5_CEU_bcm:genotype_0002
238 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA11881 CEPH1347.14 r27_ch5_CEU_bcm:genotype_0002
239 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA11882 CEPH1347.15 r27_ch5_CEU_bcm:genotype_0002
242 ss23895733 G/G PERLEGEN AFD_EUR_PANEL NA10854 71_IND_CHR_5
242 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA10854 CEPH1349.02 r27_ch5_CEU_bcm:genotype_0002
253 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA11840 CEPH1349.14 r27_ch5_CEU_bcm:genotype_0002
254 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA10856 CEPH1350.01 r27_ch5_CEU_bcm:genotype_0002
262 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA11829 CEPH1350.10 r27_ch5_CEU_bcm:genotype_0002
264 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA11831 CEPH1350.12 r27_ch5_CEU_bcm:genotype_0002
344 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA12716 CEPH1358.11 r27_ch5_CEU_bcm:genotype_0002
348 ss23895733 G/G PERLEGEN AFD_EUR_PANEL NA10860 71_IND_CHR_5
348 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA10860 CEPH1362.01 r27_ch5_CEU_bcm:genotype_0002
349 ss23895733 G/G PERLEGEN AFD_EUR_PANEL NA10861 71_IND_CHR_5
349 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA10861 CEPH1362.02 r27_ch5_CEU_bcm:genotype_0002
361 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA11993 CEPH1362.14 r27_ch5_CEU_bcm:genotype_0002
363 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA11995 CEPH1362.16 r27_ch5_CEU_bcm:genotype_0002
366 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA10863 CEPH1375.02 r27_ch5_CEU_bcm:genotype_0002
373 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12264 CEPH1375.11 r27_ch5_CEU_bcm:genotype_0002
374 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12234 CEPH1375.12 r27_ch5_CEU_bcm:genotype_0002
408 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12154 CEPH1408.10 r27_ch5_CEU_bcm:genotype_0002
429 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA10835 CEPH1416.01 r27_ch5_CEU_bcm:genotype_0002
439 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12249 CEPH1416.12 r27_ch5_CEU_bcm:genotype_0002
464 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12003 CEPH1420.09 r27_ch5_CEU_bcm:genotype_0002
465 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA12004 CEPH1420.10 r27_ch5_CEU_bcm:genotype_0002
467 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA12006 CEPH1420.12 r27_ch5_CEU_bcm:genotype_0002
524 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA12740 CEPH1444.02 r27_ch5_CEU_bcm:genotype_0002
535 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA12750 CEPH1444.13 r27_ch5_CEU_bcm:genotype_0002
536 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA12751 CEPH1444.14 r27_ch5_CEU_bcm:genotype_0002
546 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA12761 CEPH1447.10 r27_ch5_CEU_bcm:genotype_0002
547 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12762 CEPH1447.11 r27_ch5_CEU_bcm:genotype_0002
565 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12801 CEPH1454.01 r27_ch5_CEU_bcm:genotype_0002
566 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12802 CEPH1454.02 r27_ch5_CEU_bcm:genotype_0002
576 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12812 CEPH1454.12 r27_ch5_CEU_bcm:genotype_0002
610 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12864 CEPH1459.01 r27_ch5_CEU_bcm:genotype_0002
611 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12865 CEPH1459.02 r27_ch5_CEU_bcm:genotype_0002
618 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12872 CEPH1459.09 r27_ch5_CEU_bcm:genotype_0002
620 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12874 CEPH1459.11 r27_ch5_CEU_bcm:genotype_0002
621 ss44658305 G/G CSHL-HAPMAP HapMap-CEU NA12875 CEPH1459.12 r27_ch5_CEU_bcm:genotype_0002
623 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA12878 CEPH1463.02 r27_ch5_CEU_bcm:genotype_0002
636 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA12891 CEPH1463.15 r27_ch5_CEU_bcm:genotype_0002
637 ss44658305 C/C CSHL-HAPMAP HapMap-CEU NA12892 CEPH1463.16 r27_ch5_CEU_bcm:genotype_0002
5132 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA18500 YOR004.01 r27_ch5_YRI_bcm:genotype_0002
5133 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA18502 YOR004.02 r27_ch5_YRI_bcm:genotype_0002
5134 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19127 YOR077.02 r27_ch5_YRI_bcm:genotype_0002
5135 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19128 YOR077.03 r27_ch5_YRI_bcm:genotype_0002
5136 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19132 YOR101.01 r27_ch5_YRI_bcm:genotype_0002
5138 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19130 YOR101.03 r27_ch5_YRI_bcm:genotype_0002
5139 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19100 YOR105.01 r27_ch5_YRI_bcm:genotype_0002
5140 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19099 YOR105.02 r27_ch5_YRI_bcm:genotype_0002
5141 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19098 YOR105.03 r27_ch5_YRI_bcm:genotype_0002
5143 ss44658305 C/C CSHL-HAPMAP HapMap-YRI NA19193 YOR112.02 r27_ch5_YRI_bcm:genotype_0002
5145 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19240 YOR117.01 r27_ch5_YRI_bcm:genotype_0002
5146 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19238 YOR117.02 r27_ch5_YRI_bcm:genotype_0002
5150 ss44658305 G/G CSHL-HAPMAP HapMap-HCB NA18529 CH18529 r27_ch5_CHB_bcm:genotype_0002
5152 ss44658305 C/C CSHL-HAPMAP HapMap-HCB NA18532 CH18532 r27_ch5_CHB_bcm:genotype_0002
5153 ss44658305 G/G CSHL-HAPMAP HapMap-HCB NA18561 CH18561 r27_ch5_CHB_bcm:genotype_0002
5159 ss44658305 C/C CSHL-HAPMAP HapMap-HCB NA18542 CH18542 r27_ch5_CHB_bcm:genotype_0002
5160 ss44658305 C/C CSHL-HAPMAP HapMap-HCB NA18545 CH18545 r27_ch5_CHB_bcm:genotype_0002
5161 ss44658305 C/C CSHL-HAPMAP HapMap-HCB NA18572 CH18572 r27_ch5_CHB_bcm:genotype_0002
5163 ss44658305 G/G CSHL-HAPMAP HapMap-HCB NA18609 CH18609 r27_ch5_CHB_bcm:genotype_0002
5164 ss44658305 C/C CSHL-HAPMAP HapMap-HCB NA18550 CH18550 r27_ch5_CHB_bcm:genotype_0002
5165 ss44658305 G/G CSHL-HAPMAP HapMap-HCB NA18608 CH18608 r27_ch5_CHB_bcm:genotype_0002
5166 ss44658305 G/G CSHL-HAPMAP HapMap-HCB NA18552 CH18552 r27_ch5_CHB_bcm:genotype_0002
5168 ss44658305 C/C CSHL-HAPMAP HapMap-HCB NA18555 CH18555 r27_ch5_CHB_bcm:genotype_0002
5170 ss44658305 G/G CSHL-HAPMAP HapMap-HCB NA18566 CH18566 r27_ch5_CHB_bcm:genotype_0002
5172 ss44658305 G/G CSHL-HAPMAP HapMap-HCB NA18570 CH18570 r27_ch5_CHB_bcm:genotype_0002
5174 ss44658305 G/G CSHL-HAPMAP HapMap-HCB NA18571 CH18571 r27_ch5_CHB_bcm:genotype_0002
5176 ss44658305 C/C CSHL-HAPMAP HapMap-HCB NA18621 CH18621 r27_ch5_CHB_bcm:genotype_0002
5183 ss44658305 C/C CSHL-HAPMAP HapMap-HCB NA18624 CH18624 r27_ch5_CHB_bcm:genotype_0002
5185 ss44658305 C/C CSHL-HAPMAP HapMap-HCB NA18632 CH18632 r27_ch5_CHB_bcm:genotype_0002
5188 ss44658305 G/G CSHL-HAPMAP HapMap-HCB NA18635 CH18635 r27_ch5_CHB_bcm:genotype_0002
5192 ss44658305 C/C CSHL-HAPMAP HapMap-HCB NA18637 CH18637 r27_ch5_CHB_bcm:genotype_0002
5194 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18940 JA18940 r27_ch5_JPT_bcm:genotype_0002
5195 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18951 JA18951 r27_ch5_JPT_bcm:genotype_0002
5198 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18944 JA18944 r27_ch5_JPT_bcm:genotype_0002
5202 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18952 JA18952 r27_ch5_JPT_bcm:genotype_0002
5203 ss44658305 G/G CSHL-HAPMAP HapMap-JPT NA18956 JA18956 r27_ch5_JPT_bcm:genotype_0002
5204 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18964 JA18964 r27_ch5_JPT_bcm:genotype_0002
5205 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18953 JA18953 r27_ch5_JPT_bcm:genotype_0002
5207 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18959 JA18959 r27_ch5_JPT_bcm:genotype_0002
5208 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18969 JA18969 r27_ch5_JPT_bcm:genotype_0002
5209 ss44658305 G/G CSHL-HAPMAP HapMap-JPT NA18960 JA18960 r27_ch5_JPT_bcm:genotype_0002
5211 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18972 JA18972 r27_ch5_JPT_bcm:genotype_0002
5213 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18973 JA18973 r27_ch5_JPT_bcm:genotype_0002
5215 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18975 JA18975 r27_ch5_JPT_bcm:genotype_0002
5216 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18967 JA18967 r27_ch5_JPT_bcm:genotype_0002
5217 ss44658305 G/G CSHL-HAPMAP HapMap-JPT NA18976 JA18976 r27_ch5_JPT_bcm:genotype_0002
5220 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18980 JA18980 r27_ch5_JPT_bcm:genotype_0002
5221 ss44658305 G/G CSHL-HAPMAP HapMap-JPT NA18995 JA18995 r27_ch5_JPT_bcm:genotype_0002
5222 ss44658305 G/G CSHL-HAPMAP HapMap-JPT NA18981 JA18981 r27_ch5_JPT_bcm:genotype_0002
5224 ss44658305 G/G CSHL-HAPMAP HapMap-JPT NA18974 JA18974 r27_ch5_JPT_bcm:genotype_0002
5225 ss44658305 G/G CSHL-HAPMAP HapMap-JPT NA18987 JA18987 r27_ch5_JPT_bcm:genotype_0002
5227 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18991 JA18991 r27_ch5_JPT_bcm:genotype_0002
5228 ss44658305 C/C CSHL-HAPMAP HapMap-JPT NA18994 JA18994 r27_ch5_JPT_bcm:genotype_0002
5230 ss44658305 G/G CSHL-HAPMAP HapMap-JPT NA18997 JA18997 r27_ch5_JPT_bcm:genotype_0002
5231 ss44658305 G/G CSHL-HAPMAP HapMap-JPT NA18998 JA18998 r27_ch5_JPT_bcm:genotype_0002
5236 ss44658305 G/G CSHL-HAPMAP HapMap-JPT NA19003 JA19003 r27_ch5_JPT_bcm:genotype_0002
5238 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA18503 YOR005.01 r27_ch5_YRI_bcm:genotype_0002
5240 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA18504 YOR005.03 r27_ch5_YRI_bcm:genotype_0002
5245 ss44658305 C/C CSHL-HAPMAP HapMap-YRI NA18858 YOR012.02 r27_ch5_YRI_bcm:genotype_0002
5246 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA18859 YOR012.03 r27_ch5_YRI_bcm:genotype_0002
5248 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA18517 YOR013.02 r27_ch5_YRI_bcm:genotype_0002
5250 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA18521 YOR016.01 r27_ch5_YRI_bcm:genotype_0002
5252 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA18522 YOR016.03 r27_ch5_YRI_bcm:genotype_0002
5253 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA18872 YOR017.01 r27_ch5_YRI_bcm:genotype_0002
5254 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA18870 YOR017.02 r27_ch5_YRI_bcm:genotype_0002
5256 ss44658305 C/C CSHL-HAPMAP HapMap-YRI NA18854 YOR018.01 r27_ch5_YRI_bcm:genotype_0002
5258 ss44658305 C/C CSHL-HAPMAP HapMap-YRI NA18853 YOR018.03 r27_ch5_YRI_bcm:genotype_0002
5262 ss44658305 C/C CSHL-HAPMAP HapMap-YRI NA18863 YOR024.01 r27_ch5_YRI_bcm:genotype_0002
5266 ss44658305 C/C CSHL-HAPMAP HapMap-YRI NA18912 YOR028.02 r27_ch5_YRI_bcm:genotype_0002
5268 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19094 YOR040.01 r27_ch5_YRI_bcm:genotype_0002
5270 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19092 YOR040.03 r27_ch5_YRI_bcm:genotype_0002
5271 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19103 YOR042.01 r27_ch5_YRI_bcm:genotype_0002
5272 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19102 YOR042.02 r27_ch5_YRI_bcm:genotype_0002
5274 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19139 YOR043.01 r27_ch5_YRI_bcm:genotype_0002
5275 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19137 YOR043.02 r27_ch5_YRI_bcm:genotype_0002
5276 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19138 YOR043.03 r27_ch5_YRI_bcm:genotype_0002
5277 ss44658305 C/C CSHL-HAPMAP HapMap-YRI NA19202 YOR045.01 r27_ch5_YRI_bcm:genotype_0002
5282 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19171 YOR047.03 r27_ch5_YRI_bcm:genotype_0002
5286 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19211 YOR050.01 r27_ch5_YRI_bcm:genotype_0002
5287 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19209 YOR050.02 r27_ch5_YRI_bcm:genotype_0002
5288 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19210 YOR050.03 r27_ch5_YRI_bcm:genotype_0002
5289 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19208 YOR051.01 r27_ch5_YRI_bcm:genotype_0002
5290 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19206 YOR051.02 r27_ch5_YRI_bcm:genotype_0002
5291 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19207 YOR051.03 r27_ch5_YRI_bcm:genotype_0002
5292 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19161 YOR056.01 r27_ch5_YRI_bcm:genotype_0002
5294 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19160 YOR056.03 r27_ch5_YRI_bcm:genotype_0002
5296 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19222 YOR058.02 r27_ch5_YRI_bcm:genotype_0002
5299 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19116 YOR060.02 r27_ch5_YRI_bcm:genotype_0002
5300 ss44658305 C/C CSHL-HAPMAP HapMap-YRI NA19119 YOR060.03 r27_ch5_YRI_bcm:genotype_0002
5302 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19140 YOR071.02 r27_ch5_YRI_bcm:genotype_0002
5303 ss44658305 C/C CSHL-HAPMAP HapMap-YRI NA19141 YOR071.03 r27_ch5_YRI_bcm:genotype_0002
5305 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19152 YOR072.02 r27_ch5_YRI_bcm:genotype_0002
5310 ss44658305 G/G CSHL-HAPMAP HapMap-YRI NA19129 YOR077.01 r27_ch5_YRI_bcm:genotype_0002
Genotype data submitted for597 samples from582 individualsIndividual with multiple genotypes submission:15

  Validation Summary: back to top
Validation status Marker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqbySubmitterwith2hitwithHapMapFreqWith1000GenomeData
Validated by: PERLEGEN
DoubleHit found by:  BCM_SSAHASNP
UNKNOWN UNKNOWN UNKNOWN

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Revised: May 25, 2006 1:38 PM .