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rs12063142

From SNPedia

Orientationplus
Stabilizedplus
Make rs12063142(C;C)
Make rs12063142(C;T)
Make rs12063142(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position18813023
is asnp
is mentioned by
dbSNPrs12063142
ebirs12063142
HLIrs12063142
Exacrs12063142
Varsomers12063142
Maprs12063142
PheGenIrs12063142
hapmaprs12063142
1000 genomesrs12063142
hgdprs12063142
ensemblrs12063142
gopubmedrs12063142
geneviewrs12063142
scholarrs12063142
googlers12063142
pharmgkbrs12063142
gwascentralrs12063142
openSNPrs12063142
23andMers12063142
23andMe allrs12063142
SNP Nexus

SNPshotrs12063142
SNPdbers12063142
MSV3drs12063142
GWAS Ctlgrs12063142
GMAF0.2052
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20070850OA-icon.png]
Trait Parkinson's disease
Title Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
Risk Allele
P-val 5E-7
Odds Ratio None None