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rs4538475

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 1 Normal risk of developing Parkinson's Disease
(A;G) 1.5 Slightly increased risk of developing Parkinson's Disease
(G;G) 2 Increased risk of developing Parkinson's Disease
ReferenceGRCh38 38.1/141
Chromosome4
Position15736314
GeneBST1
is asnp
is mentioned by
dbSNPrs4538475
ebirs4538475
HLIrs4538475
Exacrs4538475
Varsomers4538475
Maprs4538475
PheGenIrs4538475
hapmaprs4538475
1000 genomesrs4538475
hgdprs4538475
ensemblrs4538475
gopubmedrs4538475
geneviewrs4538475
scholarrs4538475
googlers4538475
pharmgkbrs4538475
gwascentralrs4538475
openSNPrs4538475
23andMers4538475
23andMe allrs4538475
SNP Nexus

SNPshotrs4538475
SNPdbers4538475
MSV3drs4538475
GWAS Ctlgrs4538475
GMAF0.3127
Max Magnitude2
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19915576]
Trait Parkinson's disease
Title Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
Risk Allele G
P-val 3E-9
Odds Ratio 1.24 [1.16-1.34]
OMIM168600
Desc
Variant
Relatedalso


GET Evidence
rs4538475
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.293651
summary