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Reference SNP (refSNP) Cluster Report: rs2814707                 **Clinical Channel**
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:100/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqwith2hitWith1000GenomeData
Citation:PubMedLitVarNEW
Association:NHGRI GWAS
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:A/C/G (REV)
Allele Origin:
Ancestral Allele:G
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:T=0.1725/864 (1000 Genomes)
T=0.2126/26696 (TOPMED)
HGVS Names
  • CM000671.2:g.27536399C>G
  • CM000671.2:g.27536399C>T
  • NC_000009.11:g.27536397C>T
  • NC_000009.12:g.27536399C>G
  • NC_000009.12:g.27536399C>T
  • XR_001746639.1:n.7082-113G>A
  • XR_001746639.1:n.7082-113G>C
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 ss280166813 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs2814707 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
ss3986902SC_JCM|AL451123.3_64757fwd/TA/Gtggctcttgtagctaggaattccagggttgcactggctttgggcactactggatgcagga09/25/0110/10/03100Genomicunknown
ss12925684SC_SNP|NT_008413.15_27526398byFreqrev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca10/21/0310/25/06119Genomicunknown
ss15698838SC_SNP|NT_008413.16_27526397rev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca11/17/0311/22/03120Genomicunknown
ss66614796ILLUMINA|HumanHap300v1.1_rs2814707fwd/TA/Gtggctcttgtagctaggaattccagggttgcactggctttgggcactactggatgcagga11/09/0611/09/06127Genomicunknown
ss67274737ILLUMINA|HumanHap550v1.1_rs2814707fwd/TA/Gtggctcttgtagctaggaattccagggttgcactggctttgggcactactggatgcagga11/14/0611/14/06127Genomicunknown
ss67675997ILLUMINA|HumanHap650Yv1.0_rs2814707fwd/TA/Gtggctcttgtagctaggaattccagggttgcactggctttgggcactactggatgcagga11/14/0611/14/06127Genomicunknown
ss70753232ILLUMINA|HumanHap550v3.0__rs2814707rev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca04/20/0703/30/08130Genomicunknown
ss71326044ILLUMINA|HumanHap650Yv3.0_rs2814707fwd/TA/Gtggctcttgtagctaggaattccagggttgcactggctttgggcactactggatgcagga04/23/0704/23/07127Genomicunknown
ss75442971ILLUMINA|ILMN_Human_1M_rs2814707fwd/TA/Gtggctcttgtagctaggaattccagggttgcactggctttgggcactactggatgcagga08/28/0708/29/07129Genomicunknown
ss79147898ILLUMINA|HumanHap300v2.0_rs2814707fwd/TA/Gtggctcttgtagctaggaattccagggttgcactggctttgggcactactggatgcagga04/18/0711/18/07130Genomicunknown
ss84089445KRIBB_YJKIM|KHS632632fwd/TA/Gtggctcttgtagctaggaattccagggttgcactggctttgggcactactggatgcagga12/04/0712/06/07130Genomicunknown
ss104608684BGI|BGI_rs2814707rev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca06/08/0806/18/09131Genomicunknown
ss115716353ILLUMINA-UK|NA18507_000046766_NCBI36.1_chr9_27526397byFreqrev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca01/15/0909/05/14130Genomic99 %
ss122110297ILLUMINA|HumanCNV370v1_C_rs2814707fwd/TA/Gtggctcttgtagctaggaattccagggttgcactggctttgggcactactggatgcagga04/14/0904/15/09131Genomicunknown
ss154235891ILLUMINA|Human610_Quadv1_B_rs2814707-128_B_R_1501741648rev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca06/18/0906/20/09131Genomicunknown
ss159412326ILLUMINA|Human660W-Quad_v1_A_rs2814707-128_B_R_1501741648rev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca07/06/0907/07/09131Genomicunknown
ss160581472ILLUMINA|HumanOmni1-Quad_v1-0_B_rs2814707-128_B_R_1501741648rev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca08/04/0910/03/09131Genomicunknown
ss171392653ILLUMINA|HumanCNV370-Quadv3_C_rs2814707-128_B_R_1501741648rev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca10/01/0910/03/09132Genomicunknown
ss173471886ILLUMINA|Human1M-Duov3_B_rs2814707-128_B_R_1501741648rev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca10/01/0910/03/09132Genomicunknown
ss2107480391000GENOMES|YRI.trio.3.2010_874761_chr9_27526397rev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca03/29/1003/29/10132Genomicunknown
ss2241993441000GENOMES|pilot_1_YRI_6009027_chr9_27526397rev/C/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca04/22/1004/22/10132Genomicunknown
ss2347811331000GENOMES|pilot_1_CEU_4385762_chr9_27526397rev/C/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca05/01/1005/01/10132Genomicunknown
ss2415630361000GENOMES|pilot_1_CHB+JPT_3448113_chr9_27526397rev/C/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca05/01/1005/01/10132Genomicunknown
ss280166813GMI|GMI_AK_SNP_4487086rev/C/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca12/16/1012/16/10137Genomicunknown
ss285995265GMI|GMI_NA10851_SNP_2008038rev/C/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca12/17/1012/17/10138Genomicunknown
ss480670814ILLUMINA|HumanOmni2.5-4v1_B_rs2814707-128_B_R_1660354984rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag01/30/1210/29/16137Genomicunknown
ss480686312ILLUMINA|HumanOmniExpress-12v1_C_rs2814707-131_B_R_1857321009rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag01/30/1210/27/16137Genomicunknown
ss481540029ILLUMINA|HumanOmni1-Quad_v1-0_C_rs2814707-131_B_R_1865677700rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag01/30/1208/28/15146Genomicunknown
ss485130315ILLUMINA|HumanOmni2.5-4v1_D_rs2814707-131_B_R_1857321009rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag01/30/1210/28/16137Genomicunknown
ss491421497EXOME_CHIP|.GWAS._137723_chr_9_27536397rev/BC/Ttcctgcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaagagcca03/05/1203/05/12137Genomicunknown
ss537129336ILLUMINA|HumanOmni5-4v1_B_rs2814707-131_B_R_1866545294rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag06/22/1208/29/15146Genomicunknown
ss561331535TISHKOFF|snp_chr9_27536397rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag11/22/1211/23/12138Genomicunknown
ss655767569SSMP|9_27536397rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag12/14/1202/12/15138Genomicunknown
ss778507112ILLUMINA|HumanOmni25Exome-8v1_A_rs2814707-131_B_R_1866545294rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/30/1307/10/15146Genomicunknown
ss780683886ILLUMINA|HumanOmni25Exome-8v1_A_exm-rs2814707-131_B_R_1990481879rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/30/1307/10/15146Genomicunknown
ss783011468ILLUMINA|HumanOmni2.5-4v1_H_rs2814707-131_B_R_1857321009rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/30/1307/29/15142Genomicunknown
ss783357305ILLUMINA|HumanOmniExpressExome-8v1_A_exm-rs2814707-131_B_R_1990481879rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/31/1306/19/15146Genomicunknown
ss783971706ILLUMINA|HumanOmniExpressExome-8v1_A_rs2814707-131_B_R_1967900697rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/31/1306/19/15146Genomicunknown
ss825478416ILLUMINA|HumanCNV370v1_C_rs2814707-120_B_R_IFB1135296870:0rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag06/24/1311/21/14144Genomicunknown
ss832268830ILLUMINA|HumanOmniExpress-12v1_H_rs2814707-131_B_R_1857321009rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag09/17/1306/19/15144Genomicunknown
ss832923997ILLUMINA|Human660W-Quad_v1_C_rs2814707-131_B_R_1857321009rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag09/18/1307/02/15142Genomicunknown
ss833514827ILLUMINA|Human660W-Quad_v1_H_rs2814707-131_B_R_1857321009rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag09/18/1307/02/15142Genomicunknown
ss833963315ILLUMINA|HumanOmni2.5-8v1_A_rs2814707-131_B_R_1866545294rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag09/18/1307/29/15146Genomicunknown
ss986462654EVA-GONL|EVA-GONL_rs2814707rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag04/23/1404/25/14142Genomicunknown
ss1076231359JMKIDD_LAB|HGDP_WGS_chr9_27536397rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag07/10/1407/11/14142Genomicunknown
ss13334854441000GENOMES|PHASE3_V1_45973394rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag08/16/1408/16/14142Genomicunknown
ss1431795262DDI|DDI_rs2814707rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag11/04/1411/05/14144Genomicunknown
ss1583047261EVA_GENOME_DK|EVA_GENOME_DK_snv_rs2814707rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag02/19/1502/20/15144Genomicunknown
ss1596097772EVA_DECODE|EVA_DECODE_9_27526397_274392_rs2814707rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag03/02/1503/03/15144Genomicunknown
ss1622554339EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_9_27536397_25436150rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag03/04/1503/04/15144Genomicunknown
ss1665548372EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_9_27536397_25436150rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag03/04/1503/04/15144Genomicunknown
ss1713102273EVA_SVP|EVA_SVP_796640rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag03/12/1503/12/15144Genomicunknown
ss1752773725ILLUMINA|OmniExpressExome-8v1-1_B_exm-rs2814707-131_B_R_1990481879rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/27/1506/09/15146Genomicunknown
ss1752773726ILLUMINA|OmniExpressExome-8v1-1_B_rs2814707-131_B_R_1967900697rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/27/1506/09/15146Genomicunknown
ss1917835422ILLUMINA|HumanExome-12v1-1_B_exm-rs2814707-131_B_R_1990481879rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag10/16/1510/16/15147Genomicunknown
ss1929746508WEILL_CORNELL_DGM|SNV:chr9:27536397rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag10/16/1510/17/15147Genomicunknown
ss1946256135ILLUMINA|HumanCoreExome-12v1-0_C_exm-rs2814707-131_B_R_1990481879rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag10/29/1510/29/15147Genomicunknown
ss1959176048ILLUMINA|exm-rs2814707-131_B_R_1990481879rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag11/13/1511/13/15147Genomicunknown
ss1966657435AMU|chr9_27536397rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag01/29/1601/29/16147Genomicunknown
ss2025584738JJLAB|SNP6087293rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag08/29/1608/30/16149Genomicunknown
ss2094835299ILLUMINA|Immuno_BeadChip_11419691_B_rs2814707-131_B_R_1866545294rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag09/27/1609/27/16150Genomicunknown
ss2095220741ILLUMINA|InfiniumImmunoArray-24v2-0_A_rs2814707-131_B_R_1866545294rev/BC/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag09/27/1609/27/16150Genomicunknown
ss2153810338USC_VALOUEV|NC_000009.11:g.27536397C>Trev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag11/17/1611/17/16150Genomicunknown
ss2310599815HUMAN_LONGEVITY|HLI-9-27536399-C-Trev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag11/18/1611/18/16150Genomicunknown
ss2480695660TOPMED|9_27536397_C/Trev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag11/20/1611/20/16150Genomicunknown
ss2634855640ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_SoL-rs2814707-131_B_R_2131rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag02/02/1702/02/17151Genomicunknown
ss2634855641ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_rs2814707-131_B_R_19679006rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag02/02/1702/02/17151Genomicunknown
ss2634855642ILLUMINA|SoL_HCHS_Custom_15041502_B3_RefStrand_seq-rs2814707-131_B_R_2130rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag02/02/1702/02/17151Genomicunknown
ss2635194563ILLUMINA|Cancer_BeadChip_11459870_A_rs2814707-128_B_R_1660354984rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag02/02/1702/02/17151Genomicunknown
ss2709616683GRF|rs2814707rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag02/13/1702/13/17151Genomicunknown
ss2877057365GNOMAD|rs2814707rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/19/1705/19/17151Genomicunknown
ss2985459254AFFY|Axiom_PsorMich_Affx-33606852rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/24/1705/24/17151Genomicunknown
ss2986105324AFFY|Axiom_Smokesc1_Affx-33606852rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/24/1705/24/17151Genomicunknown
ss3004608969SWEGEN|NC_000009.11:g.27536397C>Trev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag05/30/1705/30/17151Genomicunknown
ss3022920561ILLUMINA|MEGA_Consortium_v2_15070954_A2_exm-rs2814707-131_B_R_1990481879rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag06/28/1706/28/17151Genomicunknown
ss3026581030BIOINF_KMB_FNS_UNIBA|9.27536399C>Trev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag07/05/1707/05/17151Genomicunknown
ss3348589769CSHL|rs2814707rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag10/02/1710/02/17151Genomicunknown
ss3585802623TOPMED|TOPMed_freeze_5?chr9:27,536,399-01rev/C/Gcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag10/07/1710/07/17151Genomicunknown
ss3585802624TOPMED|TOPMed_freeze_5?chr9:27,536,399-02rev/C/Tcatccagtagtgcccaaagccagtgcaaccctggaattcctagctacaag10/07/1710/07/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs2814707|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='A/C/G'|mol=Genomic|build=151
 ACCATCCAAG ATCTTCGGGA GGAATAGATG AACTAATGTA TGTGAAAATG TCCAGCACAG
 GTCCTAACCC ATAGTAGGTG CTCACCAAAT GTTAGTTCCC TGCCCTCCAC GTTGTGTGTA
 TCCGGAGCTG CACTAGATGC TGAGGCAAAT GGTCTCAAAT GTACTTTAAC ACTTAATGAC
 TGAGATTTTT TCTGAGCTGC CTACAGGTTA TTGACTATAT TCATTATTAA TAATAATATA
 TATGGCCACT TCAGGCAACT GGGGCTAAAT TTTGCTTGGC TCTCTAAGAA ATGTAAAGAA
 TGCCTCCTGT AATTGCTCAC CTCAAGTATT TATTCATTGG CTCTCGTGCT TTATTGGTTG
 TCCCTGAGGA CTTTAGCCCT CTCTCACTGC AGCACAGACA CTGTGCTTTC TCCTAGTTTC
 TGTGGCAAGT GACAGGAGCC CACCTCAAAC TAAAGCAAAA GGGACTTCAT TGGCTCTTGT
 AGCTAGGAAT TCCAGGGTTG
 V
 CACTGGCTTT GGGCACTACT GGATGCAGGA ATTCAAACAA TGTCTTCAAC TCTTTCTTTT
 GGTGTTTCTC TCAGCTGTGC TTCTCTTGTC GTTTCTTTTT CCCATTTTAC AGATAAGTTC
 ATCCGTAACT GAGAGAGGTG AAAAGGGGAT GGCTGCAGAG AACTCTGGCT TATATCATCC
 TTGCTTGCTG ACCTCAAGGT CCATGTATAA ATTCTCAGAG AAGAAGCCCT CTGGTTGGTG
 ATGCTTGGAA CATGCCCTGG AGGGTGGGCC CCTTGAAGTG GAGCTTGCTG GAACCACATG
 GGCTGGAGCA AGGCGCTAGG GCCAGAAGAG AGAGGTAGGC AGGGCTGCTG GCCAGGCACT
 CTTCACCAAG ACAAGGCAAG AGGAGGGGCA TGATTGAGGC AGTGATACAG AAAGCAGACA
 GTAGAGGTCG TGGCAAGTGT GCCGTTACTT GCTACCTGTG GTTGATGGGA GAGTCACACC
 ACATTTAGGA GGAGAGAATC

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_008413 AC016237 AC025611 AL139116 AL355585
dbSNP Blast Analysis
OMIM
105550

  Population Diversity (Alleles in RefSNP orientation) . See additional population frequency from 1000Genome [here] Note: rs2814707 allele is reverse to the genome back to top

Sample AscertainmentGenotype DetailAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/G
G/G
HWPA
G
ss115716353HapMap-CEUEuropean 226IG0.097345140.283185840.619469050.020022000.238938050.76106197
HapMap-HCBAsian 86IG 0.069767450.930232581.000000000.034883720.96511626
HapMap-JPTAsian 172IG 0.116279070.883720931.000000000.058139540.94186044
HapMap-YRISub-Saharan African 226IG0.026548670.300884960.672566350.751830000.176991150.82300884
HAPMAP-ASW 98IG0.040816330.285714300.673469360.751830000.183673470.81632656
HAPMAP-CHBAsian 82IG 0.097560970.902439001.000000000.048780490.95121950
HAPMAP-CHD 170IG 0.117647060.882352951.000000000.058823530.94117647
HAPMAP-GIH 176IG0.011363640.238636360.750000000.654721000.130681810.86931819
HAPMAP-LWK 180IG0.044444450.344444450.611111101.000000000.216666670.78333336
HAPMAP-MEX 100IG0.020000000.040000000.940000000.000999000.040000000.95999998
HAPMAP-MKK 286IG0.027972030.342657360.629370630.402784000.199300710.80069929
HAPMAP-TSI 176IG0.056818180.443181810.500000000.342782000.278409090.72159094
ENSEMBL_Watson 2IG 1.00000000 1.00000000
YRI 2IG 1.00000000 0.500000000.50000000
ENSEMBL_Venter 2IG 1.00000000 1.00000000
ss1333485444EAS 1008AF 0.069400000.93059999
EUR 1006AF 0.235599990.76440001
AFR 1322AF 0.223100010.77689999
AMR 694AF 0.151300000.84869999
SAS 978AF 0.160499990.83950001
ss224199344pilot_1_YRI_low_coverage_panel 118AF 0.161016960.83898306
ss234781133pilot_1_CEU_low_coverage_panel 120AF 0.216666670.78333336
ss241563036pilot_1_CHB+JPT_low_coverage_panel 120AF 0.041666670.95833331

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
Additional Freq. Data
0.286+/-0.2470000ALFRED: 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
byClusterbyFreqwith2hitWith1000GenomeData
DoubleHit found by:  BCM_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

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