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rs121908301

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121908301(A;A)
Make rs121908301(A;G)
ReferenceGRCh37 37.1/132
Chromosome1
Position155204848
GeneGBA
is asnp
is mentioned by
dbSNPrs121908301
ebirs121908301
HLIrs121908301
Exacrs121908301
Varsomers121908301
Maprs121908301
PheGenIrs121908301
hapmaprs121908301
1000 genomesrs121908301
hgdprs121908301
ensemblrs121908301
gopubmedrs121908301
geneviewrs121908301
scholarrs121908301
googlers121908301
pharmgkbrs121908301
gwascentralrs121908301
openSNPrs121908301
23andMers121908301
23andMe allrs121908301
SNP Nexus

SNPshotrs121908301
SNPdbers121908301
MSV3drs121908301
GWAS Ctlgrs121908301
Max Magnitude0
OMIM606463
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121908301(A;A)
Alt rs121908301(A;A)
Reference rs121908301(G;G)
Significance Pathogenic
Disease Gaucher's disease
Variation info
Gene GBA
CLNDBN Gaucher's disease, type 1
Reversed 1
HGVS NC_000001.10:g.155204848C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004552.4,