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rs4964469

From SNPedia

Orientationplus
Stabilizedplus
Make rs4964469(A;A)
Make rs4964469(A;G)
Make rs4964469(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position106556209
GeneRPL23P10
is asnp
is mentioned by
dbSNPrs4964469
ebirs4964469
HLIrs4964469
Exacrs4964469
Varsomers4964469
Maprs4964469
PheGenIrs4964469
hapmaprs4964469
1000 genomesrs4964469
hgdprs4964469
ensemblrs4964469
gopubmedrs4964469
geneviewrs4964469
scholarrs4964469
googlers4964469
pharmgkbrs4964469
gwascentralrs4964469
openSNPrs4964469
23andMers4964469
23andMe allrs4964469
SNP Nexus

SNPshotrs4964469
SNPdbers4964469
MSV3drs4964469
GWAS Ctlgrs4964469
GMAF0.4513
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21084426]
Trait
Title Genome-wide association study confirms BST1 and suggests a locus on 12q24 as risk loci for Parkinson's disease in the European population
Risk Allele A
P-val 2E-7
Odds Ratio 1.1600 [1.09-1.22]