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rs121908297

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121908297(A;C)
Make rs121908297(C;C)
ReferenceGRCh37 37.1/132
Chromosome1
Position155208310
GeneGBA
is asnp
is mentioned by
dbSNPrs121908297
ebirs121908297
HLIrs121908297
Exacrs121908297
Varsomers121908297
Maprs121908297
PheGenIrs121908297
hapmaprs121908297
1000 genomesrs121908297
hgdprs121908297
ensemblrs121908297
gopubmedrs121908297
geneviewrs121908297
scholarrs121908297
googlers121908297
pharmgkbrs121908297
gwascentralrs121908297
openSNPrs121908297
23andMers121908297
23andMe allrs121908297
SNP Nexus

SNPshotrs121908297
SNPdbers121908297
MSV3drs121908297
GWAS Ctlgrs121908297
Max Magnitude0
OMIM606463
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121908297(C;C)
Alt rs121908297(C;C)
Reference rs121908297(A;A)
Significance Pathogenic
Disease Gaucher's disease
Variation info
Gene GBA
CLNDBN Gaucher's disease, type 1
Reversed 1
HGVS NC_000001.10:g.155208310T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004539.4,