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rs4764478

From SNPedia

Orientationplus
Stabilizedplus
Make rs4764478(A;A)
Make rs4764478(A;T)
Make rs4764478(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position5968959
GeneVWF
is asnp
is mentioned by
dbSNPrs4764478
ebirs4764478
HLIrs4764478
Exacrs4764478
Varsomers4764478
Maprs4764478
PheGenIrs4764478
hapmaprs4764478
1000 genomesrs4764478
hgdprs4764478
ensemblrs4764478
gopubmedrs4764478
geneviewrs4764478
scholarrs4764478
googlers4764478
pharmgkbrs4764478
gwascentralrs4764478
openSNPrs4764478
23andMers4764478
23andMe allrs4764478
SNP Nexus

SNPshotrs4764478
SNPdbers4764478
MSV3drs4764478
GWAS Ctlgrs4764478
GMAF0.1763
Max Magnitude
? (A;A) (A;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


[PMID 20346360OA-icon.png] Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease.