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rs1800380

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome12
Position6029429
GeneVWF
is asnp
is mentioned by
dbSNPrs1800380
ebirs1800380
HLIrs1800380
Exacrs1800380
Varsomers1800380
Maprs1800380
PheGenIrs1800380
hapmaprs1800380
1000 genomesrs1800380
hgdprs1800380
ensemblrs1800380
gopubmedrs1800380
geneviewrs1800380
scholarrs1800380
googlers1800380
pharmgkbrs1800380
gwascentralrs1800380
openSNPrs1800380
23andMers1800380
23andMe allrs1800380
SNP Nexus

SNPshotrs1800380
SNPdbers1800380
MSV3drs1800380
GWAS Ctlgrs1800380
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 rs1800380(A;A)
Alt rs1800380(A;A)
Reference rs1800380(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene VWF
CLNDBN not specified
Reversed 1
HGVS NC_000012.11:g.6138595C>T
CLNSRC
CLNACC RCV000176272.1,