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rs121908062

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908062(G;T)
Make rs121908062(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position4933350
GeneGP1BA
is asnp
is mentioned by
dbSNPrs121908062
ebirs121908062
HLIrs121908062
Exacrs121908062
Varsomers121908062
Maprs121908062
PheGenIrs121908062
hapmaprs121908062
1000 genomesrs121908062
hgdprs121908062
ensemblrs121908062
gopubmedrs121908062
geneviewrs121908062
scholarrs121908062
googlers121908062
pharmgkbrs121908062
gwascentralrs121908062
openSNPrs121908062
23andMers121908062
23andMe allrs121908062
SNP Nexus

SNPshotrs121908062
SNPdbers121908062
MSV3drs121908062
GWAS Ctlgrs121908062
Max Magnitude0
OMIM606672
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908062(T;T)
Alt rs121908062(T;T)
Reference rs121908062(G;G)
Significance Pathogenic
Disease Pseudo von Willebrand disease
Variation info
Gene GP1BA
CLNDBN Pseudo von Willebrand disease
Reversed 0
HGVS NC_000017.10:g.4836645G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004370.2,