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rs1063857

From SNPedia

Orientationminus
Stabilizedminus
Make rs1063857(C;C)
Make rs1063857(C;T)
Make rs1063857(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position6044348
GeneVWF
is asnp
is mentioned by
dbSNPrs1063857
ebirs1063857
HLIrs1063857
Exacrs1063857
Varsomers1063857
Maprs1063857
PheGenIrs1063857
hapmaprs1063857
1000 genomesrs1063857
hgdprs1063857
ensemblrs1063857
gopubmedrs1063857
geneviewrs1063857
scholarrs1063857
googlers1063857
pharmgkbrs1063857
gwascentralrs1063857
openSNPrs1063857
23andMers1063857
23andMe allrs1063857
SNP Nexus

SNPshotrs1063857
SNPdbers1063857
MSV3drs1063857
GWAS Ctlgrs1063857
GMAF0.3434
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 20940418] Variation in the von Willebrand Factor gene is associated with VWF levels and with the risk of cardiovascular disease