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rs1800382

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1800382(A;A)
Make rs1800382(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position6019222
GeneVWF
is asnp
is mentioned by
dbSNPrs1800382
ebirs1800382
HLIrs1800382
Exacrs1800382
Varsomers1800382
Maprs1800382
PheGenIrs1800382
hapmaprs1800382
1000 genomesrs1800382
hgdprs1800382
ensemblrs1800382
gopubmedrs1800382
geneviewrs1800382
scholarrs1800382
googlers1800382
pharmgkbrs1800382
gwascentralrs1800382
openSNPrs1800382
23andMers1800382
23andMe allrs1800382
SNP Nexus

SNPshotrs1800382
SNPdbers1800382
MSV3drs1800382
GWAS Ctlgrs1800382
Max Magnitude0
OMIM613160
Desc
Variant0010
Relatedalso
ClinVar
Risk rs1800382(A;A)
Alt rs1800382(A;A)
Reference rs1800382(G;G)
Significance Non-pathogenic
Disease VON WILLEBRAND FACTOR POLYMORPHISM
Variation info
Gene VWF
CLNDBN VON WILLEBRAND FACTOR POLYMORPHISM
Reversed 1
HGVS NC_000012.11:g.6128388C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000317.2,