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rs878853315

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853315(C;G)
Make rs878853315(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
GeneGBA
is asnp
is mentioned by
dbSNPrs878853315
ebirs878853315
HLIrs878853315
Exacrs878853315
Varsomers878853315
Maprs878853315
PheGenIrs878853315
hapmaprs878853315
1000 genomesrs878853315
hgdprs878853315
ensemblrs878853315
gopubmedrs878853315
geneviewrs878853315
scholarrs878853315
googlers878853315
pharmgkbrs878853315
gwascentralrs878853315
openSNPrs878853315
23andMers878853315
23andMe allrs878853315
SNP Nexus

SNPshotrs878853315
SNPdbers878853315
MSV3drs878853315
GWAS Ctlgrs878853315
Max Magnitude0
ClinVar
Risk rs878853315(G;G)
Alt rs878853315(G;G)
Reference rs878853315(C;C)
Significance Probable-Pathogenic
Disease Gaucher's disease
Variation info
Gene GBA
CLNDBN Gaucher's disease, type 1
Reversed 1
HGVS NC_000001.10:g.155206083G>C
CLNSRC
CLNACC RCV000225396.1,