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rs80356760

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
(ACT;ACT) 0 common in clinvar
(TCA;TCA) 0 common in clinvar
Make rs80356760(-;-)
Make rs80356760(-;G)
Make rs80356760(G;G)
ReferenceGRCh37.p5 37.3/137
Chromosome1
Position155210442
GeneGBA
is asnp
is mentioned by
dbSNPrs80356760
ebirs80356760
HLIrs80356760
Exacrs80356760
Varsomers80356760
Maprs80356760
PheGenIrs80356760
hapmaprs80356760
1000 genomesrs80356760
hgdprs80356760
ensemblrs80356760
gopubmedrs80356760
geneviewrs80356760
scholarrs80356760
googlers80356760
pharmgkbrs80356760
gwascentralrs80356760
openSNPrs80356760
23andMers80356760
23andMe allrs80356760
SNP Nexus

SNPshotrs80356760
SNPdbers80356760
MSV3drs80356760
GWAS Ctlgrs80356760
Max Magnitude0
ClinVar
Risk rs80356760(G;G)
Alt rs80356760(G;G)
Reference rs80356760(TCA;TCA)
Significance Pathogenic
Disease Gaucher disease
Variation info
Gene GBA
CLNDBN Gaucher disease
Reversed 1
HGVS NC_000001.10:g.155210442_155210443insC
CLNSRC ClinVar GeneReviews
CLNACC RCV000020160.1,