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Reference SNP (refSNP) Cluster Report: rs1356888                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:88/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqwith2hitWith1000GenomeData
Citation:PubMedLitVarNEW
Association:NHGRI GWAS PheGenI
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:A/C/T (FWD)
Allele Origin:
Ancestral Allele:C
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:T=0.1420/711 (1000 Genomes)
T=0.1400/17585 (TOPMED)
HGVS Names
  • CM000664.2:g.50288880T>A
  • CM000664.2:g.50288880T>C
  • NC_000002.11:g.50516018T>C
  • NC_000002.12:g.50288880T>A
  • NC_000002.12:g.50288880T>C
  • NG_011878.1:g.748657A>G
  • NG_011878.1:g.748657A>T
  • NM_001135659.2:c.3485-51910A>G
  • NM_001135659.2:c.3485-51910A>T
  • NM_001330077.1:c.3341-51910A>G
  • NM_001330077.1:c.3341-51910A>T
  • NM_001330078.1:c.3365-51910A>G
  • NM_001330078.1:c.3365-51910A>T
  • NM_001330082.1:c.3341-51910A>G
  • NM_001330082.1:c.3341-51910A>T
  • NM_001330083.1:c.3299-51910A>G
  • NM_001330083.1:c.3299-51910A>T
  • NM_001330084.1:c.3299-51910A>G
  • NM_001330084.1:c.3299-51910A>T
  • NM_001330085.1:c.3338-51910A>G
  • NM_001330085.1:c.3338-51910A>T
  • NM_001330086.1:c.3365-51910A>G
  • NM_001330086.1:c.3365-51910A>T
  • NM_001330087.1:c.3254-51910A>G
  • NM_001330087.1:c.3254-51910A>T
  • NM_001330088.1:c.3284-51910A>G
  • NM_001330088.1:c.3284-51910A>T
  • NM_001330091.1:c.260-51910A>G
  • NM_001330091.1:c.260-51910A>T
  • NM_001330092.1:c.260-51910A>G
  • NM_001330092.1:c.260-51910A>T
  • NM_001330093.1:c.3362-51910A>G
  • NM_001330093.1:c.3362-51910A>T
  • NM_001330094.1:c.3353-51910A>G
  • NM_001330094.1:c.3353-51910A>T
  • NM_001330095.1:c.3314-51910A>G
  • NM_001330095.1:c.3314-51910A>T
  • NM_001330096.1:c.3254-51910A>G
  • NM_001330096.1:c.3254-51910A>T
  • NM_001330097.1:c.260-51910A>G
  • NM_001330097.1:c.260-51910A>T
  • NM_004801.5:c.3365-51910A>G
  • NM_004801.5:c.3365-51910A>T
  • NM_138735.4:c.260-51910A>G
  • NM_138735.4:c.260-51910A>T
Links
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 ss276463055 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs1356888 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
ss2138382TSC-CSHL|TSC0494673fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg10/19/0010/10/0388Genomic95 %
ss5178941TSC-CSHL|TSC1052549fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg09/20/0210/10/03108Genomicunknown
ss11474549WI_SSAHASNP|chr2.NT_022184.12_29331950byFreqfwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg07/03/0308/14/07116Genomicunknown
ss14499443WUGSC_SSAHASNP|chr2.NT_022184.13_29331950fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg11/05/0311/22/03119Genomicunknown
ss44302331ABI|hCV7547517fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg07/18/0507/18/05126Genomicunknown
ss66448772AFFY|SNP_A-2211240byFreqfwd/BC/Tccctaactagaagagaagctccatgaattaaa10/29/0608/14/07127Genomicunknown
ss76236639AFFY|AFFY_6_1M_SNP_A-2211240fwd/BC/Tccctaactagaagagaagctccatgaattaaa08/28/0708/30/07129Genomicunknown
ss80234933HGSV|Cor18507_SNV_20070510.chr2_50427669fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg11/23/0711/25/07130Genomicunknown
ss81462102KRIBB_YJKIM|KHS88287fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg11/30/0711/30/07130Genomicunknown
ss91157614BCMHGSC_JDW|JWB-1239935fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg02/26/0803/01/08129Genomicunknown
ss97037079HUMANGENOME_JCVI|1103658095422fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg03/28/0803/28/08130Genomicunknown
ss103494978BGI|BGI_rs1356888fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg06/06/0806/17/09131Genomicunknown
ss1095020141000GENOMES|CEU.trio.12.15.2008_375681_chr2_50369522fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg12/16/0812/16/08130Genomicunknown
ss1102473731000GENOMES|NA19240_2008_12_16_340077_chr2_50369522fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg12/17/0812/17/08130Genomicunknown
ss117701693ILLUMINA-UK|NA18507_000075226_NCBI36.1_chr2_50369522fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg01/19/0901/20/09130Genomic99 %
ss138441778ENSEMBL|ENSSNP5771143fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg05/15/0905/17/09131Genomicunknown
ss157046943GMI|GMI_SNP_46576511fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg06/24/0906/25/09131Genomicunknown
ss163427129COMPLETE_GENOMICS|NA19240_36_chr2_50369522fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg09/29/0909/29/09132Genomicunknown
ss164373053COMPLETE_GENOMICS|NA07022_36_chr2_50369522fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg09/29/0909/29/09132Genomicunknown
ss166582553COMPLETE_GENOMICS|NA20431_36_chr2_50369522fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg09/30/0909/30/09132Genomicunknown
ss172438625ILLUMINA|Human1M-Duov3_B_rs1356888-128_B_F_1518265471fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg10/01/0910/02/09132Genomicunknown
ss172922048AFFY|GenomeWideSNP_5_SNP_A-2211240fwd/BC/Tccctaactagaagagaagctccatgaattaaa10/01/0910/02/09132Genomicunknown
ss200424403BUSHMAN|BUSHMAN-chr2-50369521fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg02/16/1003/07/10132Genomicunknown
ss205696352BCM-HGSC-SUB|BCM_CMT_1011-327234fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg03/15/1003/16/10132Genomicunknown
ss2192376261000GENOMES|pilot_1_YRI_1047309_chr2_50369522fwd/C/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg04/22/1004/22/10132Genomicunknown
ss2311625331000GENOMES|pilot_1_CEU_767162_chr2_50369522fwd/C/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg05/01/1005/01/10132Genomicunknown
ss2387177191000GENOMES|pilot_1_CHB+JPT_602796_chr2_50369522fwd/C/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg05/01/1005/01/10132Genomicunknown
ss253099427BL|SNP59641_2_50369522fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg08/18/1008/18/10134Genomicunknown
ss276463055GMI|GMI_AK_SNP_783224fwd/C/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg12/16/1012/16/10137Genomicunknown
ss284343857GMI|GMI_NA10851_SNP_356624fwd/C/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg12/17/1012/17/10138Genomicunknown
ss292266290PJP|SNP_1772648_chr2_50369522fwd/C/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg01/21/1101/21/11134Genomicunknown
ss491318846EXOME_CHIP|.GWAS._35073_chr_2_50516018fwd/BC/Tggtgactgtactaaccctaactagaagagaagctccatgaattaaataatggttgaaatg03/05/1203/05/12137Genomicunknown
ss536857815ILLUMINA|HumanOmni5-4v1_B_rs1356888-131_B_F_1909642264fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg06/22/1208/28/15146Genomicunknown
ss555554676TISHKOFF|snp_chr2_50516018fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg11/22/1211/23/12138Genomicunknown
ss649137447SSMP|2_50516018fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg12/14/1202/10/15138Genomicunknown
ss780681838ILLUMINA|HumanOmni25Exome-8v1_A_exm-rs1356888-131_B_F_1990479474fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg05/30/1307/09/15142Genomicunknown
ss783355170ILLUMINA|HumanOmniExpressExome-8v1_A_exm-rs1356888-131_B_F_1990479474fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg05/31/1306/19/15142Genomicunknown
ss976810841EVA-GONL|EVA-GONL_rs1356888fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg04/23/1404/23/14142Genomicunknown
ss1069101198JMKIDD_LAB|HGDP_WGS_chr2_50516018fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg07/10/1407/10/14142Genomicunknown
ss12971481821000GENOMES|PHASE3_V1_8130986fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg08/16/1408/16/14142Genomicunknown
ss1428571938DDI|DDI_rs1356888fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg11/04/1411/04/14144Genomicunknown
ss1578871534EVA_GENOME_DK|EVA_GENOME_DK_snv_rs1356888fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg02/19/1502/20/15144Genomicunknown
ss1586221356EVA_DECODE|EVA_DECODE_2_50369522_423248_rs1356888fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg03/02/1503/02/15144Genomicunknown
ss1603469979EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_2_50516018_4496851fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg03/04/1503/04/15144Genomicunknown
ss1646464012EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_2_50516018_4496851fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg03/04/1503/04/15144Genomicunknown
ss1712454459EVA_SVP|EVA_SVP_149011fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg03/12/1503/12/15144Genomicunknown
ss1752360339ILLUMINA|OmniExpressExome-8v1-1_B_exm-rs1356888-131_B_F_1990479474fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg05/27/1506/09/15146Genomicunknown
ss1796732604HAMMER_LAB|Hsieh_872101fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg07/15/1507/15/15146Genomicunknown
ss1917749160ILLUMINA|HumanExome-12v1-1_B_exm-rs1356888-131_B_F_1990479474fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg10/16/1510/16/15147Genomicunknown
ss1920045496WEILL_CORNELL_DGM|SNV:chr2:50516018fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg10/16/1510/16/15147Genomicunknown
ss1946040224ILLUMINA|HumanCoreExome-12v1-0_C_exm-rs1356888-131_B_F_1990479474fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg10/29/1510/29/15147Genomicunknown
ss1958416658ILLUMINA|exm-rs1356888-131_B_F_1990479474fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg11/13/1511/13/15147Genomicunknown
ss1968766169GENOMED|rs1356888fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg02/16/1602/16/16147Genomicunknown
ss2020556660JJLAB|SNP1059215fwd/BC/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg08/29/1608/30/16149Genomicunknown
ss2148600367USC_VALOUEV|NC_000002.11:g.50516018T>Cfwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg11/17/1611/17/16150Genomicunknown
ss2230099917HUMAN_LONGEVITY|HLI-2-50288880-T-Cfwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg11/18/1611/18/16150Genomicunknown
ss2396031697TOPMED|2_50516018_T/Cfwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg11/19/1611/19/16150Genomicunknown
ss2624789823SYSTEMSBIOZJU|SYSTEMSBIOZJU_SNV666295fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg01/06/1701/06/17151Genomicunknown
ss2633612297ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_rs1356888-131_B_F_19096422fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg02/02/1702/02/17151Genomicunknown
ss2633612298ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_seq-rs1356888-131_B_F_2130fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg02/02/1702/02/17151Genomicunknown
ss2703166333GRF|rs1356888fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg02/13/1702/13/17151Genomicunknown
ss2773213508GNOMAD|rs1356888fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg05/17/1705/17/17151Genomicunknown
ss2985168074AFFY|Axiom_PsorMich_Affx-20179219fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg05/24/1705/24/17151Genomicunknown
ss2985794885AFFY|Axiom_Smokesc1_Affx-20179219fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg05/24/1705/24/17151Genomicunknown
ss2989469952SWEGEN|NC_000002.11:g.50516018T>Cfwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg05/30/1705/30/17151Genomicunknown
ss3021969908ILLUMINA|MEGA_Consortium_v2_15070954_A2_exm-rs1356888-131_B_F_1990479474fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg06/28/1706/28/17151Genomicunknown
ss3024044503BIOINF_KMB_FNS_UNIBA|2.50288880T>Cfwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg07/05/1707/05/17151Genomicunknown
ss3307340389TOPMED|TOPMed_freeze_5?chr2:50,288,880-01fwd/A/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg10/02/1710/02/17151Genomicunknown
ss3307340390TOPMED|TOPMed_freeze_5?chr2:50,288,880-02fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg10/02/1710/02/17151Genomicunknown
ss3344221035CSHL|rs1356888fwd/C/Tctgtactaaccctaactagaagagaagctccatgaattaaataatggttg10/02/1710/02/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs1356888|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='A/C/T'|mol=Genomic|build=151
 CCCACCCCAA AATGTCAGTA ATGCCACAGT TGAGAAACTC TCAGATAAAG ACATAAGGAT
 GACTTAAAGG GAGATAAAAA TGAAGAAAGA ATACCTTTTG TATTAGTCTA TTCTCATGCT
 GCTAATAAAG ACATACCCAA GATGGGGTAA TTTATAAAGG AAAGAGGTTT AATTGAATCA
 CAGTTCCACA TGGCTGGTGA GGCCTCACAA TCATGGCAGA AGGTGAATGA GGAGCAAAAT
 CACATCTTAC ATGGTAGCAG GCAAGAGAGA ACATGCAGGG AACTCCCATT TATAAAACCA
 TATTATCTCA TGAGACTTAT TCACTATCAC TAAAAATCAC GGGAAGGACA TGTCCCCATG
 ATTCAATCAC CTCCCACCAG TCCTTCTCAG GACACGTGGG AATTATGGGA TGTACACTTC
 AAGATGAGAT TTGGGTGGGG ACAAAGCCAA ACCATATCTC CTTTTAAAGA GGTGACTGTA
 CTAACCCTAA CTAGAAGAGA
 H
 AGCTCCATGA ATTAAATAAT GGTTGAAATG AGACGAAAAG TCAGATGCAG AGATTGTAGG
 GAAAGAGCAT AGACAGGATA CAACAATTGA GCGGCTATAA GAGAAGCTCG TAAGAAAGGT
 GAGGAATCTA GGGCAATTCC CGGGTTTCTG CTTTTGATGA CCTAGTAGCA ACTCACAGTA
 TATTGAGATA GGGAACGTAT AAGGAGAAAT AGAACTGGAT GGGAAGTTAG CTTGGTTTGG
 GAAATGACTT AGAGGAGAAT GAATAACATG TAAATGGAGC CAGTTGCAAA GAATATAATT
 ATATATGGGA ATGTGTAAAT CTGTAGAGCC CCAAGGTTAA TATTAAAAAG ACAAGAACTA
 GCCATCAAAT AAGTTGAAAT TTTACACCAT AGATATTACT ATTGACTAAA AGAGGTAGCT
 GTTAGGTGCC CTTCTCACAA TGCAAATGAG GAGTGTGGAT CTGGGTAGCT GTGATTACCC
 CCATAATGGT GAAGTTCCCC

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_022184 ABBA01075206
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
C/T
T/T
HWPC
T
ss11474549HapMap-CEUEuropean 226IG 0.663716790.300884960.035398231.000000000.814159270.18584071
HapMap-HCBAsian 86IG 0.767441870.23255815 0.751830000.883720930.11627907
HapMap-JPTAsian 172IG 0.790697690.186046510.023255810.402784000.883720930.11627907
HapMap-YRISub-Saharan African 226IG 0.796460150.185840710.017699110.583882000.889380510.11061947
HAPMAP-ASW 98IG 0.673469360.285714300.040816330.751830000.816326560.18367347
HAPMAP-CHBAsian 80IG 0.750000000.25000000 0.751830000.875000000.12500000
HAPMAP-CHD 168IG 0.678571400.297619040.023809520.751830000.827380960.17261904
HAPMAP-GIH 176IG 0.693181810.272727280.034090910.751830000.829545440.17045455
HAPMAP-LWK 180IG 0.888888900.11111111 1.000000000.944444420.05555556
HAPMAP-MEX 100IG 0.740000010.239999990.020000001.000000000.860000010.14000000
HAPMAP-MKK 286IG 0.867132840.13286713 1.000000000.933566450.06643356
HAPMAP-TSI 176IG 0.715909060.272727280.011363640.438578000.852272750.14772727
ENSEMBL_Venter 2IG 1.00000000 1.00000000
ss117701693YRI 2IG 1.00000000 0.500000000.50000000
ss1297148182EAS 1008AF 0.842300000.15769999
EUR 1006AF 0.820100010.17990001
AFR 1322AF 0.925899980.07410000
AMR 694AF 0.811199960.18880001
SAS 978AF 0.854799990.14520000
ss138441778ENSEMBL_Watson 2IG 1.00000000 0.500000000.50000000
ss163427129YRISub-Saharan African 2IG 1.00000000 1.00000000
ss164373053CEUEuropean 2IG 1.00000000 1.00000000
ss166582553PGP 2IG 1.00000000 1.00000000
ss200424403BANTU 1IG1.00000000 1.00000000
ss219237626pilot_1_YRI_low_coverage_panel 118AF 0.898305060.10169491
ss231162533pilot_1_CEU_low_coverage_panel 120AF 0.808333340.19166666
ss238717719pilot_1_CHB+JPT_low_coverage_panel 120AF 0.908333360.09166667
ss66448772HapMap-CEUEuropean 118IG 0.677966120.305084740.016949150.527089000.830508470.16949153
HapMap-HCBAsian 90IG 0.755555570.24444444 0.654721000.877777760.12222222
HapMap-JPTAsian 90IG 0.822222230.17777778 1.000000000.911111120.08888889
HapMap-YRISub-Saharan African 120IG 0.899999980.10000000 1.000000000.949999990.05000000
ss76236639ICMHP 8IG 1.00000000 1.00000000
ss97037079J. Craig Venter 2IG 1.00000000 0.500000000.50000000

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.244+/-0.2500000

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqwith2hitWith1000GenomeData
DoubleHit found by:  BCM_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

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