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Reference SNP(refSNP) Cluster Report: rs3625          
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:36/130
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/G
Ancestral Allele:G
Clinical Association:unknown
HGVS Names
NM_001135047.1:c.37A>G
NM_001135048.1:c.37A>G
NM_001135049.1:c.70A>G
NM_130469.3:c.37A>G
NP_001128519.1:p.Thr13Ala
NP_001128520.1:p.Thr13Ala
NP_001128521.1:p.Thr24Ala
NP_569736.1:p.Thr13Ala
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 ss43573334 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs3625 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
ss3660WIAF|WIAF-2388fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggcccctgac01/23/9912/23/0336cDNAunknown
ss10757052BCM_SSAHASNP|chr14.NT_026437.10_55824701byFreqfwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga06/30/0305/16/04116Genomicunknown
ss14532442WUGSC_SSAHASNP|chr14.NT_026437.10_55824701fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga11/05/0311/22/03119Genomicunknown
ss19309325CSHL-HAPMAP|CSHL-HuDD-200402.chr14.NT_026437.10_55824701fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga02/20/0403/04/04120Genomicunknown
ss24606853PERLEGEN|afd0204528byFreqfwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga08/10/0409/13/04123Genomicunknown
ss43573334ABI|hCV2200671byFreqfwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga07/18/0511/03/06126Genomicunknown
ss65727463ILLUMINA|Human1-rs3625fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga10/10/0610/10/06127Genomicunknown
ss66544051ILLUMINA|HumanHap300v1.1_rs3625fwd/BA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga11/09/0611/09/06127Genomicunknown
ss67296785ILLUMINA|HumanHap550v1.1_rs3625fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga11/14/0611/14/06127Genomicunknown
ss67701186ILLUMINA|HumanHap650Yv1.0_rs3625fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga11/14/0611/14/06127Genomicunknown
ss69162313PERLEGEN|PGP00204528byFreqfwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga01/30/0708/14/07127Genomicunknown
ss70775407ILLUMINA|HumanHap550v3.0__rs3625fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga04/20/0703/30/08130Genomicunknown
ss71351351ILLUMINA|HumanHap650Yv3.0_rs3625fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga04/23/0704/23/07127Genomicunknown
ss75472146ILLUMINA|ILMN_Human_1M_rs3625fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga08/28/0708/29/07129Genomicunknown
ss79162747ILLUMINA|HumanHap300v2.0_rs3625fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga04/18/0711/18/07130Genomicunknown
ss82989235HGSV|Cor18555_SNV_20070510.chr14_74974413fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga11/27/0712/04/07130Genomicunknown
ss83300971HGSV|Cor18956_SNV_20070510.chr14_74974413fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga11/30/0712/04/07130Genomicunknown
ss83346046KRIBB_YJKIM|KHS439801fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga12/04/0712/04/07130Genomicunknown
ss86348422CANCER-GENOME|13612fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga01/25/0801/25/08129Genomicunknown
ss89997190BCMHGSC_JDW|JWB-0794000fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga02/26/0802/29/08129Genomicunknown
ss96928641HUMANGENOME_JCVI|1103649100812fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga03/27/0803/27/08130Genomicunknown
ss106398531BGI|BGI_rs3625fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga09/15/0806/18/09130Genomicunknown
ss1084625771000GENOMES|CEU.trio.12.15.2008_3077529_chr14_74974413fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga12/15/0812/15/08130Genomicunknown
ss1135411511000GENOMES|NA19240_2008_12_16_2759480_chr14_74974413fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga12/18/0812/18/08130Genomicunknown
ss118586860ILLUMINA-UK|NA18507_000069774_NCBI36.1_chr14_74974413fwd/TA/Gcctgggcagatcccggacccttcggtgacccaggctccctgccagggcttggccccctga01/21/0901/21/09130Genomic99 %

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs3625|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 GCCTTCAAAA TAAAAAAGGC AGACACTTCT GGCAGTGCCA AGGGTGACCT TGGTGTGAGT
 TAATTGAGCA ACTTTTCCTC TATAACAGGA AGGACTTTAC GGCAGGAAGA GCAGCTGGGT
 GGGAAAGGGA TTCAGGGGAA CATTGGTGAA AGAAGCCACA GTCCTGGCAA GACGAGGGAC
 TTGAGCCCTC CTGGAGCCCC CAACCTGGCT GACTGTCCTG CTCTTTTCCT GCCCACTCCA
 GGCTGGCCTG CCACTCCTCC TGCTATGATG CCTGGGCAGA TCCCGGACCC TTCGGTGACC
 R
 CAGGCTCCCT GCCAGGGCTT GGCCCCCTGA CCGGGCTCCC CAGCTCGGCC CTGACTGTGG
 AGGAGCTGAA ATACGCTGAC ATCCGCAACC TCGGGGCCAT GATTGCACCC TTGCACTTCC
 TGGAGGTGAA ACTGGGCAAG AGGCCCCAGC CCGTGAAAAG TGAGGTGAGC GAGCCTTTTA
 CCCCTGGCAG ATTCCAGGTC TGGCCTTAAA CCCACCATGG GACCTTAACC TTGCTGTTCA
 AAGTGTGGTC TGAGGACCAG TATCATCCGT ACCACCCTGG GGTTATCAGA AATGTGGAAT

  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
dbSTS GenBank
G43530 NT_026437 ABBA01030698
dbSNP Blast Analysis
UniGene Cluster ID
196482

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss# Population Individual
Group
Chrom.
Sample Cnt.
Source A/A
A/G
G/G
HWP A
G
N
ss10757052 CEPH 184 AF 0.610 0.390
CHMJ Asian 74 IG 0.284 0.662 0.054
ss24606853 AFD_EUR_PANEL European 46 IG 0.304 0.435 0.261 0.584 0.522 0.478
AFD_AFR_PANEL African American 46 IG 0.043 0.478 0.478 0.403 0.283 0.717
AFD_CHN_PANEL Asian 48 IG 0.167 0.250 0.583 0.100 0.292 0.708
ss43573334 HapMap-CEU European 120 IG 0.250 0.450 0.300 0.479 0.475 0.525
HapMap-HCB Asian 90 IG 0.111 0.356 0.533 0.371 0.289 0.711
HapMap-JPT Asian 90 IG 0.156 0.422 0.422 0.479 0.367 0.633
HapMap-YRI Sub-Saharan African 120 IG 0.283 0.717 0.251 0.142 0.858
AoD_African_American 90 AF 0.240 0.760
AoD_Caucasian 92 AF 0.490 0.510
ss69162313 HapMap-CEU European 120 GF 0.433 0.367 0.200 0.617 0.383
HapMap-HCB Asian 90 GF 0.200 0.533 0.267 0.467 0.533
HapMap-JPT Asian 90 GF 0.267 0.489 0.244 0.511 0.489
HapMap-YRI Sub-Saharan African 120 GF 0.100 0.517 0.383 0.358 0.642
Concordant Genotype Total Sample A/A A/G G/G
ss24606853 70 12 27 30
ss43573334 1122 157 450 494
ss96928641 1 1
RefSNP Genotype Summary Total Individual A/A A/G G/G
rs3625 1264 165 472 523
Discordant Genotypes:
Indiviudal
SampleID
SubSNP(ss) Genotype Population
Handle
Submitter
Population
Submitter
SampleID
SampleID
Alias
Submission
Batch
NCBI
ProbeID
161 ss43573334 G/G CSHL-HAPMAP HapMap-CEU NA07029 CEPH1340.01 r27_ch14_CEU_illumina:human_1m_beadchip 840654
169 ss43573334 G/G CSHL-HAPMAP HapMap-CEU NA06994 CEPH1340.09 r27_ch14_CEU_illumina:human_1m_beadchip 840654
170 ss43573334 A/G CSHL-HAPMAP HapMap-CEU NA07000 CEPH1340.10 r27_ch14_CEU_illumina:human_1m_beadchip 840654
171 ss43573334 A/G CSHL-HAPMAP HapMap-CEU NA07022 CEPH1340.11 r27_ch14_CEU_illumina:human_1m_beadchip 840654
185 ss43573334 A/G CSHL-HAPMAP HapMap-CEU NA07055 CEPH1341.12 r27_ch14_CEU_illumina:human_1m_beadchip 840654
199 ss43573334 G/G CSHL-HAPMAP HapMap-CEU NA12056 CEPH1344.12 r27_ch14_CEU_illumina:human_1m_beadchip 840654
213 ss43573334 G/G CSHL-HAPMAP HapMap-CEU NA07357 CEPH1345.12 r27_ch14_CEU_illumina:human_1m_beadchip 840654
225 ss43573334 G/G CSHL-HAPMAP HapMap-CEU NA12043 CEPH1346.11 r27_ch14_CEU_illumina:human_1m_beadchip 840654
226 ss43573334 G/G CSHL-HAPMAP HapMap-CEU NA12044 CEPH1346.12 r27_ch14_CEU_illumina:human_1m_beadchip 840654
255 ss43573334 G/G CSHL-HAPMAP HapMap-CEU NA10855 CEPH1350.02 r27_ch14_CEU_illumina:human_1m_beadchip 840654
264 ss43573334 A/G CSHL-HAPMAP HapMap-CEU NA11831 CEPH1350.12 r27_ch14_CEU_illumina:human_1m_beadchip 840654
348 ss24606853 G/G PERLEGEN AFD_EUR_PANEL NA10860 71_IND_CHR_14
348 ss43573334 N/N CSHL-HAPMAP HapMap-CEU NA10860 CEPH1362.01 r27_ch14_CEU_illumina:human_1m_beadchip 840654
361 ss43573334 A/G CSHL-HAPMAP HapMap-CEU NA11993 CEPH1362.14 r27_ch14_CEU_illumina:human_1m_beadchip 840654
438 ss43573334 A/G CSHL-HAPMAP HapMap-CEU NA12248 CEPH1416.11 r27_ch14_CEU_illumina:human_1m_beadchip 840654
439 ss43573334 A/G CSHL-HAPMAP HapMap-CEU NA12249 CEPH1416.12 r27_ch14_CEU_illumina:human_1m_beadchip 840654
464 ss43573334 A/G CSHL-HAPMAP HapMap-CEU NA12003 CEPH1420.09 r27_ch14_CEU_illumina:human_1m_beadchip 840654
465 ss43573334 N/N CSHL-HAPMAP HapMap-CEU NA12004 CEPH1420.10 r27_ch14_CEU_illumina:human_1m_beadchip 840654
618 ss43573334 G/G CSHL-HAPMAP HapMap-CEU NA12872 CEPH1459.09 r27_ch14_CEU_illumina:human_1m_beadchip 840654
623 ss43573334 A/G CSHL-HAPMAP HapMap-CEU NA12878 CEPH1463.02 r27_ch14_CEU_illumina:human_1m_beadchip 840654
5135 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19128 YOR077.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5137 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19131 YOR101.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5138 ss43573334 A/G CSHL-HAPMAP HapMap-YRI NA19130 YOR101.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5140 ss43573334 A/G CSHL-HAPMAP HapMap-YRI NA19099 YOR105.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5144 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19192 YOR112.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5149 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18524 CH18524 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5154 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18562 CH18562 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5162 ss43573334 N/N CSHL-HAPMAP HapMap-HCB NA18547 CH18547 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5163 ss43573334 A/G CSHL-HAPMAP HapMap-HCB NA18609 CH18609 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5165 ss43573334 A/G CSHL-HAPMAP HapMap-HCB NA18608 CH18608 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5168 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18555 CH18555 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5170 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18566 CH18566 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5171 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18563 CH18563 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5172 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18570 CH18570 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5173 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18612 CH18612 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5175 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18620 CH18620 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5179 ss43573334 A/G CSHL-HAPMAP HapMap-HCB NA18573 CH18573 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5182 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18577 CH18577 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5188 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18635 CH18635 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5190 ss43573334 A/G CSHL-HAPMAP HapMap-HCB NA18636 CH18636 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5191 ss43573334 G/G CSHL-HAPMAP HapMap-HCB NA18593 CH18593 r27_ch14_CHB_illumina:human_1m_beadchip 840654
5200 ss43573334 G/G CSHL-HAPMAP HapMap-JPT NA18949 JA18949 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5204 ss43573334 G/G CSHL-HAPMAP HapMap-JPT NA18964 JA18964 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5207 ss43573334 A/G CSHL-HAPMAP HapMap-JPT NA18959 JA18959 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5210 ss43573334 G/G CSHL-HAPMAP HapMap-JPT NA18961 JA18961 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5211 ss43573334 A/G CSHL-HAPMAP HapMap-JPT NA18972 JA18972 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5212 ss43573334 A/G CSHL-HAPMAP HapMap-JPT NA18965 JA18965 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5213 ss43573334 G/G CSHL-HAPMAP HapMap-JPT NA18973 JA18973 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5215 ss43573334 G/G CSHL-HAPMAP HapMap-JPT NA18975 JA18975 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5217 ss43573334 G/G CSHL-HAPMAP HapMap-JPT NA18976 JA18976 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5223 ss43573334 A/G CSHL-HAPMAP HapMap-JPT NA18971 JA18971 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5226 ss43573334 G/G CSHL-HAPMAP HapMap-JPT NA18990 JA18990 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5235 ss43573334 G/G CSHL-HAPMAP HapMap-JPT NA19007 JA19007 r27_ch14_JPT_illumina:human_1m_beadchip 840654
5237 ss43573334 A/G CSHL-HAPMAP HapMap-YRI NA18501 YOR004.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5238 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18503 YOR005.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5239 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18505 YOR005.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5240 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18504 YOR005.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5241 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18506 YOR009.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5242 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18508 YOR009.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5243 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18507 YOR009.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5245 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18858 YOR012.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5248 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18517 YOR013.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5249 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18516 YOR013.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5256 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18854 YOR018.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5257 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18852 YOR018.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5259 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18857 YOR023.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5262 ss43573334 A/G CSHL-HAPMAP HapMap-YRI NA18863 YOR024.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5263 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18861 YOR024.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5264 ss43573334 A/G CSHL-HAPMAP HapMap-YRI NA18862 YOR024.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5265 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18914 YOR028.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5266 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18912 YOR028.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5267 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA18913 YOR028.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5270 ss43573334 N/N CSHL-HAPMAP HapMap-YRI NA19092 YOR040.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5274 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19139 YOR043.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5276 ss43573334 A/G CSHL-HAPMAP HapMap-YRI NA19138 YOR043.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5283 ss43573334 N/N CSHL-HAPMAP HapMap-YRI NA19205 YOR048.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5284 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19204 YOR048.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5289 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19208 YOR051.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5290 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19206 YOR051.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5294 ss43573334 A/G CSHL-HAPMAP HapMap-YRI NA19160 YOR056.03 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5295 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19221 YOR058.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5296 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19222 YOR058.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5302 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19140 YOR071.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5307 ss43573334 N/N CSHL-HAPMAP HapMap-YRI NA19145 YOR074.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5308 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19143 YOR074.02 r27_ch14_YRI_illumina:human_1m_beadchip 840654
5310 ss43573334 G/G CSHL-HAPMAP HapMap-YRI NA19129 YOR077.01 r27_ch14_YRI_illumina:human_1m_beadchip 840654
Genotype data submitted for1279 samples from1264 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 .