NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Reference SNP (refSNP) Cluster Report: rs10743149                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:120/147
Map to Genome Build:107/Weight 1
Validation Status:byClusterbyFreqwith2hitwithHapMapFreqWith1000GenomeData
Citation:PubMed
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:C/T (FWD)
Allele Origin:
Ancestral Allele:C
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:T=0.0829/415 (1000 Genomes)
HGVS Names
  • NC_000011.10:g.2172945T>C
  • NC_000011.9:g.2194175T>C
  • NG_008128.1:g.3861A>G
  • NM_000360.3:c.-1159A>G
  • NM_199292.2:c.-1159A>G
  • NM_199293.2:c.-1159A>G
  • NR_039834.1:n.-118T>C
  • XM_005253099.1:c.-1159A>G
  • XM_005253100.1:c.-1159A>G
  • XM_005253101.1:c.-1159A>G
  • XM_011520335.1:c.-1159A>G
Links , Linkout
SNP Details are organized in the following sections:
GeneView Map Submission Fasta Resource Diversity Validation

  Integrated Maps (Hint: click on 'Chr Pos' to see variant in the new NCBI variation viewer) back to top

  GeneView back to top

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


  Submitter records for this RefSNP Cluster back to top
The submission ss280852520 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs10743149 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
ss16104593SC_SNP|NT_009237.16_958115byFreqfwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga11/18/0310/26/06120Genomicunknown
ss16316417JDRF_WT_DIL|DIL944fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga11/25/0311/27/03120Genomicunknown
ss18468722SC_SNP|SC-CHR9-12_NA11321-200402.chr11.NT_009237.16_958115fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga02/20/0403/04/04120Genomicunknown
ss19202389CSHL-HAPMAP|CSHL-HuDD-200402.chr11.NT_009237.16_958115fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga02/20/0403/04/04120Genomicunknown
ss19911051CSHL-HAPMAP|CSHL-HuFF-200402.chr11.NT_009237.16_958115fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga02/21/0403/04/04120Genomicunknown
ss20780813SSAHASNP|WGSA-200403-chr11.chr11.NT_009237.16_958115fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga03/19/0403/19/04121Genomicunknown
ss67009054ILLUMINA|HumanHap650Yv1.0_rs10743149fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga11/14/0611/14/06127Genomicunknown
ss69306577PERLEGEN|PGP07347412byFreqfwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga01/30/0703/31/08127Genomicunknown
ss71018505ILLUMINA|HumanHap650Yv3.0_rs10743149fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga04/23/0704/23/07127Genomicunknown
ss75406064ILLUMINA|ILMN_Human_1M_rs10743149fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga08/28/0708/29/07129Genomicunknown
ss88430173BCMHGSC_JDW|JWB-0363641byFreqfwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga02/26/0809/05/14129Genomicunknown
ss97356023HUMANGENOME_JCVI|1103649586835fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga03/29/0803/29/08130Genomicunknown
ss106716068BGI|BGI_rs10743149fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga09/16/0810/20/09130Genomicunknown
ss1099098971000GENOMES|CEU.trio.12.15.2008_2470421_chr11_2150751fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga12/16/0812/16/08130Genomicunknown
ss1140946081000GENOMES|NA19240_2008_12_16_2228806_chr11_2150751fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga12/18/0812/18/08130Genomicunknown
ss118448451ILLUMINA-UK|NA18507_000002668_NCBI36.1_chr11_2150751fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga01/21/0902/05/09130Genomic99 %
ss119626141KRIBB_YJKIM|KHS1788388fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga02/04/0902/05/09131Genomicunknown
ss132234586ENSEMBL|ENSSNP6988400fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga05/11/0905/13/09131Genomicunknown
ss137780991ENSEMBL|ENSSNP538954fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga12/08/0810/16/09131Genomicunknown
ss155819846GMI|GMI_SNP_70243088fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga06/24/0906/24/09131Genomicunknown
ss167647875COMPLETE_GENOMICS|NA07022_36_chr11_2150751fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga09/30/0909/30/09132Genomicunknown
ss168860725COMPLETE_GENOMICS|NA19240_36_chr11_2150751fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga10/01/0910/01/09132Genomicunknown
ss170273530COMPLETE_GENOMICS|NA20431_36_chr11_2150751fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga10/01/0910/05/09132Genomicunknown
ss170433810ILLUMINA|Human1M-Duov3_B_rs10743149-128_T_R_1502305449rev/TA/Gtccctctgtacagtccagcattgtcaaggcggctctggccatctctgctgaccccagagg10/01/0910/01/09132Genomicunknown
ss202297962BUSHMAN|BUSHMAN-chr11-2150750fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga02/16/1003/08/10132Genomicunknown
ss207867852BCM-HGSC-SUB|BCM_CMT_1011-2246571fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga03/15/1003/19/10132Genomicunknown
ss2250509521000GENOMES|pilot_1_YRI_6860635_chr11_2150751fwd/C/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga04/22/1004/22/10132Genomicunknown
ss2354155581000GENOMES|pilot_1_CEU_5020187_chr11_2150751fwd/C/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga05/01/1005/01/10132Genomicunknown
ss2420760111000GENOMES|pilot_1_CHB+JPT_3961088_chr11_2150751fwd/C/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga05/01/1005/01/10132Genomicunknown
ss244269837ILLUMINA|CVDSNP55v1_A_rs10743149rev/TA/Gtccctctgtacagtccagcattgtcaaggcggctctggccatctctgctgaccccagagg06/10/1006/10/10132Genomicunknown
ss254823441BL|SNP3696_11_2150751fwd/BC/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga08/19/1008/19/10134Genomicunknown
ss280852520GMI|GMI_AK_SNP_5172873fwd/C/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga12/16/1012/16/10137Genomicunknown
ss286300330GMI|GMI_NA10851_SNP_2313115fwd/C/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga12/17/1012/17/10138Genomicunknown
ss291031398PJP|SNP_537756_chr11_2150751fwd/C/Tcctctggggtcagcagagatggccagagccgccttgacaatgctggactgtacagaggga01/21/1101/21/11134Genomicunknown
ss410888332ILLUMINA|Cardio-Metabo_Chip_11395247_A_rs10743149rev/TA/Gtccctctgtacagtccagcattgtcaaggcggctctggccatctctgctgaccccagagg06/07/1106/07/11135Genomicunknown
ss482795168ILLUMINA|HumanOmni2.5-4v1_B_SNP11-2150751-0_T_R_1613058861rev/TA/Gtccctctgtacagtccagcattgtcaaggcgnnnnnggccatctctgctgaccccagagg01/30/1202/02/12137Genomicunknown
ss484216444ILLUMINA|HumanOmni2.5-4v1_D_kgp9128669-0_T_R_1798469040rev/TA/Gtccctctgtacagtccagcattgtcaaggcggctctggccatctctgctgaccccagagg01/30/1202/03/12137Genomicunknown
ss536403330ILLUMINA|HumanOmni5-4v1_B__kgp9128669-0_T_R_1798469040fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag06/22/1208/29/15146Genomicunknown
ss562336136TISHKOFF|snp_chr11_2194175fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag11/22/1211/23/12138Genomicunknown
ss657666109SSMP|11_2194175fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag12/14/1202/12/15138Genomicunknown
ss782554241ILLUMINA|HumanOmni2.5-4v1_H_kgp9128669-0_T_R_1798469040fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag05/30/1307/29/15146Genomicunknown
ss836062977ILLUMINA|HumanOmni2.5-8v1_A_kgp9128669-0_T_R_1798469040fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag09/18/1307/29/15146Genomicunknown
ss988129836EVA-GONL|EVA-GONL_rs10743149fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag04/23/1404/25/14142Genomicunknown
ss1077445647JMKIDD_LAB|HGDP_WGS_chr11_2194175fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag07/10/1407/12/14142Genomicunknown
ss13398352321000GENOMES|PHASE3_V1_52586007fwd/C/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag08/16/1408/16/14142Genomicunknown
ss1426509142DDI|DDI_rs10743149fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag11/04/1411/04/14144Genomicunknown
ss1575475330EVA_GENOME_DK|EVA_GENOME_DK_snv_rs10743149fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag02/19/1502/19/15144Genomicunknown
ss1597808191EVA_DECODE|EVA_DECODE_11_2150751_17968_rs10743149fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag03/02/1503/04/15144Genomicunknown
ss1625847718EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_11_2194175_29060091fwd/C/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag03/04/1503/04/15144Genomicunknown
ss1668841751EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_11_2194175_29060091fwd/C/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag03/04/1503/04/15144Genomicunknown
ss1713227358EVA_SVP|EVA_SVP_921725fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag03/12/1503/12/15144Genomicunknown
ss1806659171HAMMER_LAB|Hsieh_5678272fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag07/15/1507/16/15146Genomicunknown
ss1931491727WEILL_CORNELL_DGM|SNV:chr11:2194175fwd/BC/Tggggtcagcagagatggccagagccgccttgacaatgctggactgtacag10/16/1510/17/15147Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs10743149|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=147
 GGAGACGCCA CGCGTTTCCA AATGGCTGCC ACCTCCTGCA TCACAGTCCC CACCAGGGTT
 GCCAGGGCGA CCAGGGCCAG GGACGGCTTC CACCCACCCC ACTCAGCCCC TCTATGGCCC
 ACTGCTAGCT CCTGGCTTCC CTCGGGGTCC TGTGGCCCCT TCTTTAAAGA GCACGCACGT
 CCCTCAGTGC TGAGGGCCCT GATGCCTTCC CCTTGGAGAG ACCTTTGCAG TTTCTCCTCT
 ACCCCACCAG GCCCCGGGTT GAGGGTGACC CTGGGGTGAC CTGAGAACTC CCTTGAGGAC
 AACCCCAGCC TAGAGCCTCC CCCAAGTTCC ATGTCCGCCC CGCAGGCACC CGCATCCAGC
 CCACGCCCAC TGGCACCTCC TGCTCCCAGC CGCTGCCCCA CCCAGGGAGA GTGATGCCCC
 TGCCCAGGGT GGCTTCTGGC CCTTCTGGTG GAAGGGGAGG CCTCCCCATC CCTCTGGGGT
 CAGCAGAGAT GGCCAGAGCC
 Y
 GCCTTGACAA TGCTGGACTG TACAGAGGGA AGGACGTGGC CCCAGAGTGC ATGGCCTGCG
 GCTGAACGCT GCCACCGCTG TCCCTCCTGG AGAAGAACCG TTTCCGACAG GGCTTGGGGC
 TTCCTGTATC TGCTGGGCTT TCTGGTGTTG GCAGCCCAAG ATGACACCCT GGGCCCAGCA
 GGAGCCAGAA GCCCTAGACG CTCCCTGACT TCTCGAAGGC CTACCCCGGC TGGTCACTGT
 GGCAGCCAGA GCTGGCATCT CTCAGGGCCC ACTCTGCTCC TGTCAGCTGT GGGACTCCCC
 GCTCCCCGTT CTCTCTTCAA CAATAGCCCC TGGGACCTTT CCTAAAACTG CTTCAGCCAT
 GGCATCCCTG TCCCACACCC CTCCGTGGCT CCTCGCTGCC CTCTGCAGGC AGGCTGAGTG
 CTCAGTCAAA GCAAAGGGAA GACCCCCCAA CCCTTCCCAC TTCCTGGCCC AGAAGGATTT
 GGGGCTCCGT GATCCCCGGT

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_009237 ABBA01032100
dbSNP Blast Analysis

  Population Diversity (Alleles in RefSNP orientation) . See additional population frequency from 1000Genome [here] back to top

Sample AscertainmentGenotype DetailAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceC/C
C/T
T/T
HWPC
T
ss118448451YRI 2IG1.00000000 1.00000000
ss132234586ENSEMBL_Watson 2IG1.00000000 1.00000000
ss1339835232EAS 1008AF 0.964299980.03570000
EUR 1006AF 0.887699960.11230000
AFR 1322AF 0.855499980.14450000
AMR 694AF 0.925100030.07490000
SAS 978AF 0.976500030.02350000
ss137780991ENSEMBL_Venter 2IG1.00000000 1.00000000
ENSEMBL_celera 2IG1.00000000 1.00000000
ss167647875CEUEuropean 2IG1.00000000 1.00000000
ss168860725YRISub-Saharan African 2IG1.00000000 1.00000000
ss170273530PGP 2IG 1.00000000 0.500000000.50000000
ss225050952pilot_1_YRI_low_coverage_panel 118AF 0.923728820.07627118
ss235415558pilot_1_CEU_low_coverage_panel 120AF 0.858333350.14166667
ss242076011pilot_1_CHB+JPT_low_coverage_panel 120AF 0.949999990.05000000
ss88430173HapMap-CEUEuropean 226IG0.805309710.185840710.008849561.000000000.898230080.10176991
HapMap-HCBAsian 86IG0.906976760.09302326 1.000000000.953488350.04651163
HapMap-JPTAsian 172IG0.895348850.10465116 1.000000000.947674390.05232558
HapMap-YRISub-Saharan African 226IG0.796460150.194690270.008849561.000000000.893805330.10619469
HAPMAP-ASW 98IG0.775510190.204081640.020408160.751830000.877551020.12244898
HAPMAP-CHBAsian 82IG0.951219500.04878049 1.000000000.975609780.02439024
HAPMAP-CHD 170IG0.894117650.10588235 1.000000000.947058800.05294118
HAPMAP-GIH 176IG0.931818190.06818182 1.000000000.965909060.03409091
HAPMAP-LWK 180IG0.577777800.366666670.055555561.000000000.761111140.23888889
HAPMAP-MEX 100IG0.839999970.16000000 1.000000000.920000020.08000000
HAPMAP-MKK 286IG0.762237790.209790210.027972030.294266000.867132840.13286713
HAPMAP-TSI 176IG0.772727250.215909090.011363641.000000000.880681810.11931818
ss97356023J. Craig Venter 2IG1.00000000 1.00000000
Concordant GenotypeTotal SampleCC/CC/TT/T
ss11844845111
ss13223458611
ss13778099122
ss16886072511
ss17027353011
ss20229796233
ss88430173116691421914
ss9735602311
RefSNP Genotype SummaryTotal IndividualCC/CC/TT/T
rs107431491216391922014
Discordant Genotypes:
Indiviudal
SampleID
SubSNP(ss)GenotypePopulation
Handle
Submitter
Population
Submitter
SampleID
SampleID
Alias
Submission
Batch
NCBI
ProbeID
162ss88430173N/NCSHL-HAPMAPHapMap-CEUNA07019CEPH1340.02r27_ch11_CEU_illumina:human_1m_beadchip
171ss88430173C/CCSHL-HAPMAPHapMap-CEUNA07022CEPH1340.11r27_ch11_CEU_illumina:human_1m_beadchip
171ss167647875C/CCOMPLETE_GENOMICSCEUNA07022NA07022NA07022_snpinduse_chr11
187ss88430173C/CCSHL-HAPMAPHapMap-CEUNA06985CEPH1341.14r27_ch11_CEU_illumina:human_1m_beadchip
215ss88430173N/NCSHL-HAPMAPHapMap-CEUNA10857CEPH1346.01r27_ch11_CEU_illumina:human_1m_beadchip
225ss88430173C/CCSHL-HAPMAPHapMap-CEUNA12043CEPH1346.11r27_ch11_CEU_illumina:human_1m_beadchip
344ss88430173C/CCSHL-HAPMAPHapMap-CEUNA12716CEPH1358.11r27_ch11_CEU_illumina:human_1m_beadchip
361ss88430173C/CCSHL-HAPMAPHapMap-CEUNA11993CEPH1362.14r27_ch11_CEU_illumina:human_1m_beadchip
465ss88430173N/NCSHL-HAPMAPHapMap-CEUNA12004CEPH1420.10r27_ch11_CEU_illumina:human_1m_beadchip
535ss88430173C/CCSHL-HAPMAPHapMap-CEUNA12750CEPH1444.13r27_ch11_CEU_illumina:human_1m_beadchip
546ss88430173C/CCSHL-HAPMAPHapMap-CEUNA12761CEPH1447.10r27_ch11_CEU_illumina:human_1m_beadchip
621ss88430173C/CCSHL-HAPMAPHapMap-CEUNA12875CEPH1459.12r27_ch11_CEU_illumina:human_1m_beadchip
5142ss88430173C/CCSHL-HAPMAPHapMap-YRINA19194YOR112.01r27_ch11_YRI_illumina:human_1m_beadchip
5158ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18605CH18605r27_ch11_CHB_illumina:human_1m_beadchip
5161ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18572CH18572r27_ch11_CHB_illumina:human_1m_beadchip
5162ss88430173N/NCSHL-HAPMAPHapMap-HCBNA18547CH18547r27_ch11_CHB_illumina:human_1m_beadchip
5166ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18552CH18552r27_ch11_CHB_illumina:human_1m_beadchip
5171ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18563CH18563r27_ch11_CHB_illumina:human_1m_beadchip
5176ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18621CH18621r27_ch11_CHB_illumina:human_1m_beadchip
5177ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18594CH18594r27_ch11_CHB_illumina:human_1m_beadchip
5178ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18622CH18622r27_ch11_CHB_illumina:human_1m_beadchip
5179ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18573CH18573r27_ch11_CHB_illumina:human_1m_beadchip
5183ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18624CH18624r27_ch11_CHB_illumina:human_1m_beadchip
5184ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18579CH18579r27_ch11_CHB_illumina:human_1m_beadchip
5186ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18582CH18582r27_ch11_CHB_illumina:human_1m_beadchip
5192ss88430173C/CCSHL-HAPMAPHapMap-HCBNA18637CH18637r27_ch11_CHB_illumina:human_1m_beadchip
5199ss88430173C/CCSHL-HAPMAPHapMap-JPTNA18945JA18945r27_ch11_JPT_illumina:human_1m_beadchip
5200ss88430173C/CCSHL-HAPMAPHapMap-JPTNA18949JA18949r27_ch11_JPT_illumina:human_1m_beadchip
5201ss88430173C/CCSHL-HAPMAPHapMap-JPTNA18948JA18948r27_ch11_JPT_illumina:human_1m_beadchip
5204ss88430173C/CCSHL-HAPMAPHapMap-JPTNA18964JA18964r27_ch11_JPT_illumina:human_1m_beadchip
5205ss88430173C/CCSHL-HAPMAPHapMap-JPTNA18953JA18953r27_ch11_JPT_illumina:human_1m_beadchip
5215ss88430173C/CCSHL-HAPMAPHapMap-JPTNA18975JA18975r27_ch11_JPT_illumina:human_1m_beadchip
5222ss88430173C/CCSHL-HAPMAPHapMap-JPTNA18981JA18981r27_ch11_JPT_illumina:human_1m_beadchip
5223ss88430173C/CCSHL-HAPMAPHapMap-JPTNA18971JA18971r27_ch11_JPT_illumina:human_1m_beadchip
5241ss88430173C/CCSHL-HAPMAPHapMap-YRINA18506YOR009.01r27_ch11_YRI_illumina:human_1m_beadchip
5256ss88430173C/CCSHL-HAPMAPHapMap-YRINA18854YOR018.01r27_ch11_YRI_illumina:human_1m_beadchip
5257ss88430173C/CCSHL-HAPMAPHapMap-YRINA18852YOR018.02r27_ch11_YRI_illumina:human_1m_beadchip
5267ss88430173C/CCSHL-HAPMAPHapMap-YRINA18913YOR028.03r27_ch11_YRI_illumina:human_1m_beadchip
5272ss88430173C/CCSHL-HAPMAPHapMap-YRINA19102YOR042.02r27_ch11_YRI_illumina:human_1m_beadchip
5286ss88430173C/CCSHL-HAPMAPHapMap-YRINA19211YOR050.01r27_ch11_YRI_illumina:human_1m_beadchip
5294ss88430173C/CCSHL-HAPMAPHapMap-YRINA19160YOR056.03r27_ch11_YRI_illumina:human_1m_beadchip
5297ss88430173C/TCSHL-HAPMAPHapMap-YRINA19223YOR058.03r27_ch11_YRI_illumina:human_1m_beadchip
Genotype data submitted for1218 samples from1216 individualsIndividual with multiple genotypes submission:2

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqwith2hitwithHapMapFreqWith1000GenomeData
DoubleHit found by:  BCM_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

GENERAL: Contact Us | Homepage | Announcements |dbSNP Summary | Genome | FTP SERVER | Build History | Handle Request
DOCUMENTATION: FAQ | Searchable FAQ Archive | Overview | How to Submit | RefSNP Summary Info | Database Schema
SEARCH: Entrez SNP | Blast SNP | Batch Query | By Submitter |New Batches | Method | Population | Publication | Batch | Locus Info | Between Marker
NCBI: PubMed | Entrez | BLAST | OMIM | Taxonomy | Structure

Disclaimer     Privacy statement