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Reference SNP (refSNP) Cluster Report: rs11241713                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:120/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqwith2hitwithHapMapFreqWith1000GenomeData
Citation:PubMedLitVarNEW
Association:NHGRI GWAS
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:A/C (FWD)
Allele Origin:
Ancestral Allele:C
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:A=0.2272/1138 (1000 Genomes)
A=0.1239/15557 (TOPMED)
HGVS Names
  • CM000667.2:g.123783871C>A
  • NC_000005.9:g.123119565C>A
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 ss278462259 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs11241713 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
ss19614581CSHL-HAPMAP|CSHL-HuDD-200402.chr5.NT_034772.5_25534578fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct02/20/0403/04/04120Genomicunknown
ss20233192CSHL-HAPMAP|CSHL-HuFF-200402.chr5.NT_034772.5_25534578fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct02/21/0403/04/04120Genomicunknown
ss23927253PERLEGEN|afd3603419byFreqfwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct08/10/0409/13/04123Genomicunknown
ss44593672ABI|hCV3062909byFreqfwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct07/19/0511/03/06126Genomicunknown
ss66497988AFFY|SNP_A-4201756byFreqrev/BG/Ttgatttccagagaagtaaagtagagtaccggg10/29/0603/31/08127Genomicunknown
ss66668100ILLUMINA|HumanHap300v1.1_rs11241713fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct11/09/0611/09/06127Genomicunknown
ss66928671ILLUMINA|HumanHap550v1.1_rs11241713fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct11/14/0611/14/06127Genomicunknown
ss67084320ILLUMINA|HumanHap650Yv1.0_rs11241713fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct11/14/0611/14/06127Genomicunknown
ss68948362PERLEGEN|PGP03603419byFreqfwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct01/30/0703/31/08127Genomicunknown
ss70392793ILLUMINA|HumanHap300v2.0_rs11241713fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct04/18/0711/18/07127Genomicunknown
ss70526644ILLUMINA|HumanHap550v3.0__rs11241713rev/BG/Tagagcttagatacatgatttccagagaagtaaagtagagtaccgggtggtaatgatggtt04/20/0703/30/08130Genomicunknown
ss71056685ILLUMINA|HumanHap650Yv3.0_rs11241713fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct04/23/0704/23/07127Genomicunknown
ss75610691ILLUMINA|ILMN_Human_1M_rs11241713fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct08/28/0708/29/07129Genomicunknown
ss76320973AFFY|AFFY_6_1M_SNP_A-4201756rev/BG/Ttgatttccagagaagtaaagtagagtaccggg08/28/0708/30/07129Genomicunknown
ss78255616HGSV|Cor12878_SNV_20070510.chr5_123147464fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct10/17/0710/18/07129Genomicunknown
ss85093459KRIBB_YJKIM|KHS896911fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct12/04/0712/08/07130Genomicunknown
ss105949064BGI|BGI_rs11241713fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct09/12/0806/18/09130Genomicunknown
ss1093825331000GENOMES|CEU.trio.12.15.2008_1354518_chr5_123147464fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct12/16/0812/16/08130Genomicunknown
ss121464925ILLUMINA|HumanCNV370v1_C_rs11241713fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct04/14/0904/14/09131Genomicunknown
ss152974616ILLUMINA|Human610_Quadv1_B_rs11241713-127_B_R_1501627277rev/BG/Tagagcttagatacatgatttccagagaagtaaagtagagtaccgggtggtaatgatggtt06/18/0906/19/09131Genomicunknown
ss155978049GMI|GMI_SNP_94263897fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct06/24/0906/24/09131Genomicunknown
ss159172646ILLUMINA|Human660W-Quad_v1_A_rs11241713-128_B_R_1501627277rev/BG/Tagagcttagatacatgatttccagagaagtaaagtagagtaccgggtggtaatgatggtt07/06/0907/06/09131Genomicunknown
ss159973936ILLUMINA|HumanOmni1-Quad_v1-0_B_rs11241713-128_B_R_1501627277rev/BG/Tagagcttagatacatgatttccagagaagtaaagtagagtaccgggtggtaatgatggtt08/04/0910/01/09131Genomicunknown
ss169839681ILLUMINA|HumanCNV370-Quadv3_C_rs11241713-127_B_R_1501627277rev/BG/Tagagcttagatacatgatttccagagaagtaaagtagagtaccgggtggtaatgatggtt10/01/0910/02/09132Genomicunknown
ss171208653ILLUMINA|Human1M-Duov3_B_rs11241713-127_B_R_1501627277rev/BG/Tagagcttagatacatgatttccagagaagtaaagtagagtaccgggtggtaatgatggtt10/01/0910/01/09132Genomicunknown
ss173251696AFFY|GenomeWideSNP_5_SNP_A-4201756rev/BG/Ttgatttccagagaagtaaagtagagtaccggg10/01/0910/03/09132Genomicunknown
ss206860159BCM-HGSC-SUB|BCM_CMT_1011-1086668fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct03/15/1003/18/10132Genomicunknown
ss2117067561000GENOMES|YRI.trio.3.2010_542502_chr5_123147464fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct03/29/1003/30/10132Genomicunknown
ss2219365991000GENOMES|pilot_1_YRI_3746282_chr5_123147464fwd/A/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct04/22/1004/22/10132Genomicunknown
ss2331299661000GENOMES|pilot_1_CEU_2734595_chr5_123147464fwd/A/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct05/01/1005/01/10132Genomicunknown
ss2402544581000GENOMES|pilot_1_CHB+JPT_2139535_chr5_123147464fwd/A/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct05/01/1005/01/10132Genomicunknown
ss278462259GMI|GMI_AK_SNP_2782498fwd/A/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct12/16/1012/16/10137Genomicunknown
ss285255828GMI|GMI_NA10851_SNP_1268601fwd/A/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct12/17/1012/17/10138Genomicunknown
ss293451299PJP|SNP_2957657_chr5_123147464fwd/A/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct01/21/1101/21/11134Genomicunknown
ss479508759ILLUMINA|HumanOmni2.5-4v1_B_rs11241713-128_B_R_1772929166fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa01/30/1210/28/16137Genomicunknown
ss479512702ILLUMINA|HumanOmniExpress-12v1_C_rs11241713-131_B_R_1857260090fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa01/30/1210/27/16137Genomicunknown
ss479961509ILLUMINA|HumanOmni1-Quad_v1-0_C_rs11241713-131_B_R_1865158534fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa01/30/1208/28/15146Genomicunknown
ss484553645ILLUMINA|HumanOmni2.5-4v1_D_rs11241713-131_B_R_1857260090fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa01/30/1210/28/16137Genomicunknown
ss491370202EXOME_CHIP|.GWAS._86429_chr_5_123119565fwd/TA/Caaccatcattaccacccggtactctactttacttctctggaaatcatgtatctaagctct03/05/1203/05/12137Genomicunknown
ss536690718ILLUMINA|HumanOmni5-4v1_B_rs11241713-131_B_R_1885470446fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa06/22/1208/29/15146Genomicunknown
ss558681063TISHKOFF|snp_chr5_123119565fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa11/22/1211/23/12138Genomicunknown
ss652576556SSMP|5_123119565fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa12/14/1202/11/15138Genomicunknown
ss778381935ILLUMINA|HumanOmni25Exome-8v1_A_rs11241713-131_B_R_1865158534fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa05/30/1307/09/15146Genomicunknown
ss780681023ILLUMINA|HumanOmni25Exome-8v1_A_exm-rs11241713-131_B_R_1990478512fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa05/30/1307/09/15146Genomicunknown
ss782723481ILLUMINA|HumanOmni2.5-4v1_H_rs11241713-131_B_R_1857260090fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa05/30/1307/28/15146Genomicunknown
ss783354321ILLUMINA|HumanOmniExpressExome-8v1_A_exm-rs11241713-131_B_R_1990478512fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa05/31/1306/19/15146Genomicunknown
ss783690976ILLUMINA|HumanOmniExpressExome-8v1_A_rs11241713-131_B_R_1885470446fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa05/31/1306/19/15146Genomicunknown
ss825362188ILLUMINA|HumanCNV370v1_C_rs11241713-126_B_R_IFB1135801344:0fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa06/24/1311/21/14144Genomicunknown
ss831975108ILLUMINA|HumanOmniExpress-12v1_H_rs11241713-131_B_R_1857260090fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa09/17/1306/18/15146Genomicunknown
ss833836918ILLUMINA|HumanOmni2.5-8v1_A_rs11241713-131_B_R_1865158534fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa09/18/1307/28/15146Genomicunknown
ss982069139EVA-GONL|EVA-GONL_rs11241713fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa04/23/1404/24/14142Genomicunknown
ss1073002223JMKIDD_LAB|HGDP_WGS_chr5_123119565fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa07/10/1407/11/14142Genomicunknown
ss13170031401000GENOMES|PHASE3_V1_28823675fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa08/16/1408/16/14142Genomicunknown
ss1581330336EVA_GENOME_DK|EVA_GENOME_DK_snv_rs11241713fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa02/19/1502/20/15144Genomicunknown
ss1591593540EVA_DECODE|EVA_DECODE_5_123147464_924242_rs11241713fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa03/02/1503/03/15144Genomicunknown
ss1613896618EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_5_123119565_15945585fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa03/04/1503/04/15144Genomicunknown
ss1656890651EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_5_123119565_15945585fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa03/04/1503/04/15144Genomicunknown
ss1712796420EVA_SVP|EVA_SVP_490787fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa03/12/1503/12/15144Genomicunknown
ss1752545989ILLUMINA|OmniExpressExome-8v1-1_B_rs11241713-131_B_R_1885470446fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa05/27/1506/09/15146Genomicunknown
ss1804059268HAMMER_LAB|Hsieh_3067925fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa07/15/1507/15/15146Genomicunknown
ss1917793216ILLUMINA|HumanExome-12v1-1_B_exm-rs11241713-131_B_R_1990478512fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa10/16/1510/16/15147Genomicunknown
ss1925325144WEILL_CORNELL_DGM|SNV:chr5:123119565fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa10/16/1510/17/15147Genomicunknown
ss1958818590ILLUMINA|exm-rs11241713-131_B_R_1990478512fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa11/13/1511/13/15147Genomicunknown
ss1970198041GENOMED|rs11241713fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa02/16/1602/16/16147Genomicunknown
ss2023268303JJLAB|SNP3770858fwd/TA/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa08/29/1608/30/16149Genomicunknown
ss2151424615USC_VALOUEV|NC_000005.9:g.123119565C>Afwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa11/17/1611/17/16150Genomicunknown
ss2446003840TOPMED|5_123119565_C/Afwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa11/20/1611/20/16150Genomicunknown
ss2626122838SYSTEMSBIOZJU|SYSTEMSBIOZJU_SNV2413353fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa01/06/1701/06/17151Genomicunknown
ss2634333431ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_rs11241713-131_B_R_1885470fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa02/02/1702/02/17151Genomicunknown
ss2634333432ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_seq-rs11241713-131_B_R_213fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa02/02/1702/02/17151Genomicunknown
ss2635148775ILLUMINA|Cancer_BeadChip_11459870_A_rs11241713-128_B_R_1772929166fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa02/02/1702/02/17151Genomicunknown
ss2706984734GRF|rs11241713fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa02/13/1702/13/17151Genomicunknown
ss2830156877GNOMAD|rs11241713fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa05/18/1705/18/17151Genomicunknown
ss2985332910AFFY|Axiom_PsorMich_Affx-25534190fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa05/24/1705/24/17151Genomicunknown
ss2997708394SWEGEN|NC_000005.9:g.123119565C>Afwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa05/30/1705/30/17151Genomicunknown
ss3025417272BIOINF_KMB_FNS_UNIBA|5.123783871C>Afwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa07/05/1707/05/17151Genomicunknown
ss3346604592CSHL|rs11241713fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa10/02/1710/02/17151Genomicunknown
ss3477254727TOPMED|TOPMed_freeze_5?chr5:123,783,871fwd/A/Ctcattaccacccggtactctactttacttctctggaaatcatgtatctaa10/04/1710/04/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs11241713|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='A/C'|mol=Genomic|build=151
 AAGGTGTGAG AGTTAACCAT ATGGGAGGAA AGCTGGAGAA AATTCCTTGG GAAGGTGAAA
 GGGGAGGGGT CCCAGGGCAC AAGTGGAAGG GCTGGGTTTT GACAGGTAAA TTTTCCATTT
 TATCAAAATA GAATATGGGA ACATGCTATT GTCAATACCT CACTTAAGTC AGATAGCCTG
 TATGTCTTCT GCCTTCTTCA TACTTGTAAA AGAAATTCAT ACTTTCTGCC TAAGTTAGTC
 ATACTTTGGC TCTAGTTCCA AACTATTCTT CTCACAATCA ATTGAATAAC TTTATGAATT
 CCTAGTCCCG AATTATCCTT TTTCTCTTTT CTAAATGGAA AATTCTAGTT AAGTGCTCCT
 AGTTATATTT GTCTTTTCTT GGCTGATTTT TACCTGTTTG CTTCAAAATG TGTCTCCTTT
 TTTGCCTGGT GGATTCTCCA GATCTCTCAT TTTTTTTTTT TTAACTGCTC AACCATCATT
 ACCACCCGGT ACTCTACTTT
 M
 ACTTCTCTGG AAATCATGTA TCTAAGCTCT CAGCTCTGAA CCACCTGTTT AACTTGTTAT
 TAATATAATC ATTTTCTCTG AATACTTTGA TTTCTCTGAC CCATATCAAA CTGCCCTGTT
 TTGATGGTTA TCAAGAGAGC TTAATGTCAT CACTGTCTAG TTTTTCTTAG CTATTTGATT
 TAACTGATGC CACCAACAGA TATTTGTTGA GTGCCTTCTG TGTGCCAGAC AGTGTGTCAG
 ACAGTGTGTT AGGTGATGAG TTGTATTTAT ATTTATCATA ACAACAAATA TTGACTTCCT
 TTTAACACAG TTAATTATCT TCATCTTTAC TCTCTCTCCC TGCCACTGTT TGACTTTATT
 ATTTGAATCC TAAAGTGTGA TGCTTCCTAT ATTTTGTTTA GTATTTTAAT TTGTTTCAGG
 TAGGGGGATA AACCTGGTCC TGGTTACTCT ATCATGGCCA AAAGCAGAAG TCTCAGATTA
 TGTTTTAAAA CATGTACATG

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_034772
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.
SourceA/A
A/C
C/C
HWPA
C
ss1317003140EAS 1008AF 0.560500030.43950000
EUR 1006AF 0.076500000.92350000
AFR 1322AF 0.080200000.91979998
AMR 694AF 0.213299990.78670001
SAS 978AF 0.247400000.75260001
ss221936599pilot_1_YRI_low_coverage_panel 118AF 0.059322030.94067794
ss233129966pilot_1_CEU_low_coverage_panel 120AF 0.050000000.94999999
ss23927253AFD_EUR_PANELEuropean 46IG 0.130434780.869565191.000000000.065217390.93478262
AFD_AFR_PANELAfrican American 46IG0.043478260.130434780.826086940.150222000.108695650.89130437
AFD_CHN_PANELAsian 48IG0.333333340.291666660.375000000.050043000.479166660.52083331
ss240254458pilot_1_CHB+JPT_low_coverage_panel 120AF 0.533333360.46666667
ss44593672HapMap-CEUEuropean 226IG0.008849560.115044250.876106200.479500000.066371680.93362832
HapMap-HCBAsian 86IG0.139534890.604651150.255813960.150222000.441860470.55813956
HapMap-JPTAsian 168IG0.238095240.488095220.273809521.000000000.482142870.51785713
HapMap-YRISub-Saharan African 222IG0.009009010.117117110.873873890.479500000.067567560.93243241
HAPMAP-ASW 98IG0.020408160.204081640.775510190.751830000.122448980.87755102
HAPMAP-CHBAsian 76IG0.289473680.605263170.105263160.150222000.592105270.40789473
HAPMAP-CHD 166IG0.361445780.530120490.108433740.250592000.626506030.37349397
HAPMAP-GIH 174IG0.034482760.344827590.620689630.654721000.206896560.79310346
HAPMAP-LWK 172IG0.011627910.186046510.802325611.000000000.104651160.89534885
HAPMAP-MEX 100IG0.040000000.300000010.660000031.000000000.190000000.81000000
HAPMAP-MKK 280IG0.007142860.328571440.664285720.099721000.171428580.82857144
HAPMAP-TSI 176IG 0.136363640.863636371.000000000.068181820.93181819
ss66497988HapMap-CEUEuropean 118IG0.016949150.118644070.864406760.250592000.076271180.92372882
HapMap-HCBAsian 90IG0.155555560.600000020.244444440.200325000.455555560.54444444
HapMap-JPTAsian 90IG0.311111120.444444450.244444440.479500000.533333360.46666667
HapMap-YRISub-Saharan African 120IG0.016666670.133333340.850000020.342782000.083333340.91666669
ss68948362HapMap-CEUEuropean 120IG0.033333340.116666670.850000020.025056000.091666670.90833336
HapMap-HCBAsian 90IG0.155555560.600000020.244444440.200325000.455555560.54444444
HapMap-JPTAsian 90IG0.311111120.444444450.244444440.479500000.533333360.46666667
HapMap-YRISub-Saharan African 120IG0.016666670.133333340.850000020.342782000.083333340.91666669
ss76320973ICMHP 10IG 1.00000000 1.00000000

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
Additional Freq. Data
0.351+/-0.2290000ALFRED: The Allele Frequency Database

  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

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