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rs28934879

From SNPedia

Merged intors121964895
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0
Make rs28934879(A;A)
Make rs28934879(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position6021960
GeneVWF
is asnp
is mentioned by
dbSNPrs28934879
ebirs28934879
HLIrs28934879
Exacrs28934879
Varsomers28934879
Maprs28934879
PheGenIrs28934879
hapmaprs28934879
1000 genomesrs28934879
hgdprs28934879
ensemblrs28934879
gopubmedrs28934879
geneviewrs28934879
scholarrs28934879
googlers28934879
pharmgkbrs28934879
gwascentralrs28934879
openSNPrs28934879
23andMers28934879
23andMe allrs28934879
SNP Nexus

SNPshotrs28934879
SNPdbers28934879
MSV3drs28934879
GWAS Ctlgrs28934879
StatusMerged into rs121964895
Max Magnitude0
OMIM193400
DescVON WILLEBRAND DISEASE, TYPE IIM
Variant0027
Relatedalso