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rs4130047

From SNPedia

Orientationplus
Stabilizedplus
Make rs4130047(C;C)
Make rs4130047(C;T)
Make rs4130047(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position43098270
GeneRIT2
is asnp
is mentioned by
dbSNPrs4130047
ebirs4130047
HLIrs4130047
Exacrs4130047
Varsomers4130047
Maprs4130047
PheGenIrs4130047
hapmaprs4130047
1000 genomesrs4130047
hgdprs4130047
ensemblrs4130047
gopubmedrs4130047
geneviewrs4130047
scholarrs4130047
googlers4130047
pharmgkbrs4130047
gwascentralrs4130047
openSNPrs4130047
23andMers4130047
23andMe allrs4130047
SNP Nexus

SNPshotrs4130047
SNPdbers4130047
MSV3drs4130047
GWAS Ctlgrs4130047
GMAF0.3301
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21738487OA-icon.png]
Trait
Title Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease.
Risk Allele C
P-val 2E-7
Odds Ratio 1.1600 [1.10-1.23]