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rs12456492

From SNPedia

Orientationplus
Stabilizedplus
Make rs12456492(A;A)
Make rs12456492(A;G)
Make rs12456492(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position43093415
GeneRIT2
is asnp
is mentioned by
dbSNPrs12456492
dbSNP (classic)rs12456492
ClinGenrs12456492
ebirs12456492
HLIrs12456492
Exacrs12456492
Gnomadrs12456492
Varsomers12456492
LitVarrs12456492
Maprs12456492
PheGenIrs12456492
Biobankrs12456492
1000 genomesrs12456492
hgdprs12456492
ensemblrs12456492
geneviewrs12456492
scholarrs12456492
googlers12456492
pharmgkbrs12456492
gwascentralrs12456492
openSNPrs12456492
23andMers12456492
SNPshotrs12456492
SNPdbers12456492
MSV3drs12456492
GWAS Ctlgrs12456492
GMAF0.3384
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 22451204OA-icon.png] Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2


[PMID 26188085] RIT2 rs12456492 polymorphism and the risk of Parkinson's disease: A meta-analysis