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rs77829017

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs77829017(A;A)
Make rs77829017(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position155209730
GeneGBA
is asnp
is mentioned by
dbSNPrs77829017
ebirs77829017
HLIrs77829017
Exacrs77829017
Varsomers77829017
Maprs77829017
PheGenIrs77829017
hapmaprs77829017
1000 genomesrs77829017
hgdprs77829017
ensemblrs77829017
gopubmedrs77829017
geneviewrs77829017
scholarrs77829017
googlers77829017
pharmgkbrs77829017
gwascentralrs77829017
openSNPrs77829017
23andMers77829017
23andMe allrs77829017
SNP Nexus

SNPshotrs77829017
SNPdbers77829017
MSV3drs77829017
GWAS Ctlgrs77829017
Max Magnitude0
OMIM606463
Desc
Variant0025
Relatedalso
ClinVar
Risk rs77829017(A;A)
Alt rs77829017(A;A)
Reference rs77829017(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.155209730C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004532.4,