Have questions? Visit https://www.reddit.com/r/SNPedia

rs2363337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
(C;T) 3 Von Willebrand disease, type 1 (likely)
(T;T) 3 Von Willebrand disease, type 1 (likely)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position6023630
GeneVWF
is asnp
is mentioned by
dbSNPrs2363337
ebirs2363337
HLIrs2363337
Exacrs2363337
Varsomers2363337
Maprs2363337
PheGenIrs2363337
hapmaprs2363337
1000 genomesrs2363337
hgdprs2363337
ensemblrs2363337
gopubmedrs2363337
geneviewrs2363337
scholarrs2363337
googlers2363337
pharmgkbrs2363337
gwascentralrs2363337
openSNPrs2363337
23andMers2363337
23andMe allrs2363337
SNP Nexus

SNPshotrs2363337
SNPdbers2363337
MSV3drs2363337
GWAS Ctlgrs2363337
Max Magnitude3
rs2363337, also known as c.3379+1G>A, is a SNP in the VWF gene on chromosome 12.

The rarer rs2363337(T) allele is considered likely to cause Von Willebrand disease, type 1, according to one publication.[PMID 17080221]

ClinVar
Risk rs2363337(T;T)
Alt rs2363337(T;T)
Reference rs2363337(C;C)
Significance Untested
Disease not provided
Variation info
Gene VWF
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.6132796C>T
CLNSRC
CLNACC RCV000086650.1,