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rs2229446

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2229446(A;A)
Make rs2229446(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position5993906
GeneVWF
is asnp
is mentioned by
dbSNPrs2229446
ebirs2229446
HLIrs2229446
Exacrs2229446
Varsomers2229446
Maprs2229446
PheGenIrs2229446
hapmaprs2229446
1000 genomesrs2229446
hgdprs2229446
ensemblrs2229446
gopubmedrs2229446
geneviewrs2229446
scholarrs2229446
googlers2229446
pharmgkbrs2229446
gwascentralrs2229446
openSNPrs2229446
23andMers2229446
23andMe allrs2229446
SNP Nexus

SNPshotrs2229446
SNPdbers2229446
MSV3drs2229446
GWAS Ctlgrs2229446
Max Magnitude0

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


ClinVar
Risk rs2229446(A;A)
Alt rs2229446(A;A)
Reference rs2229446(G;G)
Significance Untested
Disease not provided
Variation info
Gene VWF
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.6103072C>T
CLNSRC
CLNACC RCV000086855.1,