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rs61751290

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 3 Von Willebrand disease, type 1 (likely)
(A;G) 3 Von Willebrand disease, type 1 (likely)
(G;G) 0 common/normal
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position5976110
GeneVWF
is asnp
is mentioned by
dbSNPrs61751290
ebirs61751290
HLIrs61751290
Exacrs61751290
Varsomers61751290
Maprs61751290
PheGenIrs61751290
hapmaprs61751290
1000 genomesrs61751290
hgdprs61751290
ensemblrs61751290
gopubmedrs61751290
geneviewrs61751290
scholarrs61751290
googlers61751290
pharmgkbrs61751290
gwascentralrs61751290
openSNPrs61751290
23andMers61751290
23andMe allrs61751290
SNP Nexus

SNPshotrs61751290
SNPdbers61751290
MSV3drs61751290
GWAS Ctlgrs61751290
Max Magnitude3
rs61751290, also known as c.7437+1G>A, is a SNP in the VWF gene on chromosome 12.

The rarer rs61751290(A) allele is considered likely to cause Von Willebrand disease, type 1, according to one publication.[PMID 17080221]

ClinVar
Risk rs61751290(A,T;A,T)
Alt rs61751290(A,T;A,T)
Reference rs61751290(G;G)
Significance Untested
Disease not provided
Variation info
Gene VWF
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.6085276C>T
CLNSRC
CLNACC RCV000086885.1,