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rs7965413

From SNPedia

Orientationplus
Stabilizedplus
Make rs7965413(C;C)
Make rs7965413(C;T)
Make rs7965413(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position6125723
GeneVWF
is asnp
is mentioned by
dbSNPrs7965413
ebirs7965413
HLIrs7965413
Exacrs7965413
Varsomers7965413
Maprs7965413
PheGenIrs7965413
hapmaprs7965413
1000 genomesrs7965413
hgdprs7965413
ensemblrs7965413
gopubmedrs7965413
geneviewrs7965413
scholarrs7965413
googlers7965413
pharmgkbrs7965413
gwascentralrs7965413
openSNPrs7965413
23andMers7965413
23andMe allrs7965413
SNP Nexus

SNPshotrs7965413
SNPdbers7965413
MSV3drs7965413
GWAS Ctlgrs7965413
Max Magnitude

[PMID 25646961OA-icon.png] Identification of an Interaction between VWF rs7965413 and Platelet Count as a Novel Risk Marker for Metabolic Syndrome: An Extensive Search of Candidate Polymorphisms in a Case-Control Study