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rs7962217

From SNPedia

Orientationplus
Stabilizedplus
Make rs7962217(C;C)
Make rs7962217(C;T)
Make rs7962217(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position5952393
GeneVWF
is asnp
is mentioned by
dbSNPrs7962217
ebirs7962217
HLIrs7962217
Exacrs7962217
Varsomers7962217
Maprs7962217
PheGenIrs7962217
hapmaprs7962217
1000 genomesrs7962217
hgdprs7962217
ensemblrs7962217
gopubmedrs7962217
geneviewrs7962217
scholarrs7962217
googlers7962217
pharmgkbrs7962217
gwascentralrs7962217
openSNPrs7962217
23andMers7962217
23andMe allrs7962217
SNP Nexus

SNPshotrs7962217
SNPdbers7962217
MSV3drs7962217
GWAS Ctlgrs7962217
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25779970] Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans