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rs878853316

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853316(C;T)
Make rs878853316(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
GeneGBA
is asnp
is mentioned by
dbSNPrs878853316
ebirs878853316
HLIrs878853316
Exacrs878853316
Varsomers878853316
Maprs878853316
PheGenIrs878853316
hapmaprs878853316
1000 genomesrs878853316
hgdprs878853316
ensemblrs878853316
gopubmedrs878853316
geneviewrs878853316
scholarrs878853316
googlers878853316
pharmgkbrs878853316
gwascentralrs878853316
openSNPrs878853316
23andMers878853316
23andMe allrs878853316
SNP Nexus

SNPshotrs878853316
SNPdbers878853316
MSV3drs878853316
GWAS Ctlgrs878853316
Max Magnitude0
ClinVar
Risk rs878853316(T;T)
Alt rs878853316(T;T)
Reference rs878853316(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.155209454G>A
CLNSRC
CLNACC RCV000225500.1,