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rs12431733

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 1 Normal risk of developing Parkinson's Disease
(C;T) 1.5 Slightly increased risk of developing Parkinson's Disease
(T;T) 2 Increased risk of developing Parkinson's Disease
ReferenceGRCh38 38.1/141
Chromosome14
Position53824112
is asnp
is mentioned by
dbSNPrs12431733
ebirs12431733
HLIrs12431733
Exacrs12431733
Varsomers12431733
Maprs12431733
PheGenIrs12431733
hapmaprs12431733
1000 genomesrs12431733
hgdprs12431733
ensemblrs12431733
gopubmedrs12431733
geneviewrs12431733
scholarrs12431733
googlers12431733
pharmgkbrs12431733
gwascentralrs12431733
openSNPrs12431733
23andMers12431733
23andMe allrs12431733
SNP Nexus

SNPshotrs12431733
SNPdbers12431733
MSV3drs12431733
GWAS Ctlgrs12431733
GMAF0.3742
Max Magnitude2
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19915575OA-icon.png]
Trait Parkinson's disease
Title Genome-wide association study reveals genetic risk underlying Parkinson's disease
Risk Allele T
P-val 0.000003
Odds Ratio 1.13 [NR]


GET Evidence
rs12431733
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.390625
summary