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rs121908064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908064(A;G)
Make rs121908064(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position4933367
GeneGP1BA
is asnp
is mentioned by
dbSNPrs121908064
ebirs121908064
HLIrs121908064
Exacrs121908064
Varsomers121908064
Maprs121908064
PheGenIrs121908064
hapmaprs121908064
1000 genomesrs121908064
hgdprs121908064
ensemblrs121908064
gopubmedrs121908064
geneviewrs121908064
scholarrs121908064
googlers121908064
pharmgkbrs121908064
gwascentralrs121908064
openSNPrs121908064
23andMers121908064
23andMe allrs121908064
SNP Nexus

SNPshotrs121908064
SNPdbers121908064
MSV3drs121908064
GWAS Ctlgrs121908064
Max Magnitude0
OMIM606672
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908064(G;G)
Alt rs121908064(G;G)
Reference rs121908064(A;A)
Significance Pathogenic
Disease Pseudo von Willebrand disease
Variation info
Gene GP1BA
CLNDBN Pseudo von Willebrand disease
Reversed 0
HGVS NC_000017.10:g.4836662A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004372.2,