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rs169713

From SNPedia

Orientationplus
Stabilizedplus
Make rs169713(C;C)
Make rs169713(C;T)
Make rs169713(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position11920284
is asnp
is mentioned by
dbSNPrs169713
ebirs169713
HLIrs169713
Exacrs169713
Varsomers169713
Maprs169713
PheGenIrs169713
hapmaprs169713
1000 genomesrs169713
hgdprs169713
ensemblrs169713
gopubmedrs169713
geneviewrs169713
scholarrs169713
googlers169713
pharmgkbrs169713
gwascentralrs169713
openSNPrs169713
23andMers169713
23andMe allrs169713
SNP Nexus

SNPshotrs169713
SNPdbers169713
MSV3drs169713
GWAS Ctlgrs169713
GMAF0.287
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20226436OA-icon.png] A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1
OMIM188050
Desc
Variant
Relatedalso