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rs878853314

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853314(C;C)
Make rs878853314(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
GeneGBA
is asnp
is mentioned by
dbSNPrs878853314
ebirs878853314
HLIrs878853314
Exacrs878853314
Varsomers878853314
Maprs878853314
PheGenIrs878853314
hapmaprs878853314
1000 genomesrs878853314
hgdprs878853314
ensemblrs878853314
gopubmedrs878853314
geneviewrs878853314
scholarrs878853314
googlers878853314
pharmgkbrs878853314
gwascentralrs878853314
openSNPrs878853314
23andMers878853314
23andMe allrs878853314
SNP Nexus

SNPshotrs878853314
SNPdbers878853314
MSV3drs878853314
GWAS Ctlgrs878853314
Max Magnitude0
ClinVar
Risk rs878853314(C;C)
Alt rs878853314(C;C)
Reference rs878853314(G;G)
Significance Probable-Pathogenic
Disease Gaucher's disease
Variation info
Gene GBA
CLNDBN Gaucher's disease, type 1
Reversed 1
HGVS NC_000001.10:g.155209446C>G
CLNSRC
CLNACC RCV000225581.1,