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rs9697983

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9697983(G;G)
Make rs9697983(G;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position121049176
GeneGLUD2
is asnp
is mentioned by
dbSNPrs9697983
ebirs9697983
HLIrs9697983
Exacrs9697983
Varsomers9697983
Maprs9697983
PheGenIrs9697983
hapmaprs9697983
1000 genomesrs9697983
hgdprs9697983
ensemblrs9697983
gopubmedrs9697983
geneviewrs9697983
scholarrs9697983
googlers9697983
pharmgkbrs9697983
gwascentralrs9697983
openSNPrs9697983
23andMers9697983
23andMe allrs9697983
SNP Nexus

SNPshotrs9697983
SNPdbers9697983
MSV3drs9697983
GWAS Ctlgrs9697983
Max Magnitude0
? (G;G) (G;T) (T;T) 28
ClinVar
Risk rs9697983(G;G)
Alt rs9697983(G;G)
Reference rs9697983(T;T)
Significance Pathogenic
Disease Parkinson disease
Variation info
Gene GLUD2
CLNDBN Parkinson disease, late-onset
Reversed 0
HGVS NC_000023.10:g.120183030T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022827.24,