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rs61748906

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61748906(A;G)
Make rs61748906(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position155238228
GeneGBA
is asnp
is mentioned by
dbSNPrs61748906
ebirs61748906
HLIrs61748906
Exacrs61748906
Varsomers61748906
Maprs61748906
PheGenIrs61748906
hapmaprs61748906
1000 genomesrs61748906
hgdprs61748906
ensemblrs61748906
gopubmedrs61748906
geneviewrs61748906
scholarrs61748906
googlers61748906
pharmgkbrs61748906
gwascentralrs61748906
openSNPrs61748906
23andMers61748906
23andMe allrs61748906
SNP Nexus

SNPshotrs61748906
SNPdbers61748906
MSV3drs61748906
GWAS Ctlgrs61748906
Max Magnitude0
ClinVar
Risk rs61748906(G;G)
Alt rs61748906(G;G)
Reference rs61748906(A;A)
Significance Pathogenic
Disease not provided Gaucher's disease
Variation info
Gene GBA
CLNDBN not provided Gaucher's disease, type 1
Reversed 0
HGVS NC_000001.10:g.155208019A>G
CLNSRC HGMD
CLNACC RCV000079351.3, RCV000179795.1,