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rs121908306

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs121908306(G;G)
Make rs121908306(G;T)
ReferenceGRCh37 37.1/132
Chromosome1
Position155206119
GeneGBA
is asnp
is mentioned by
dbSNPrs121908306
ebirs121908306
HLIrs121908306
Exacrs121908306
Varsomers121908306
Maprs121908306
PheGenIrs121908306
hapmaprs121908306
1000 genomesrs121908306
hgdprs121908306
ensemblrs121908306
gopubmedrs121908306
geneviewrs121908306
scholarrs121908306
googlers121908306
pharmgkbrs121908306
gwascentralrs121908306
openSNPrs121908306
23andMers121908306
23andMe allrs121908306
SNP Nexus

SNPshotrs121908306
SNPdbers121908306
MSV3drs121908306
GWAS Ctlgrs121908306
Max Magnitude0
OMIM606463
Desc
Variant0031
Relatedalso
ClinVar
Risk rs121908306(G;G)
Alt rs121908306(G;G)
Reference rs121908306(T;T)
Significance Pathogenic
Disease Acute neuronopathic Gaucher's disease
Variation info
Gene GBA
CLNDBN Acute neuronopathic Gaucher's disease
Reversed 1
HGVS NC_000001.10:g.155206119A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004563.2,