rs4538475
From SNPedia
Orientation | plus |
Stabilized | plus |
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 |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 15736314 |
Gene | BST1 |
is a | snp |
is | mentioned by |
dbSNP | rs4538475 |
dbSNP (classic) | rs4538475 |
ClinGen | rs4538475 |
ebi | rs4538475 |
HLI | rs4538475 |
Exac | rs4538475 |
Gnomad | rs4538475 |
Varsome | rs4538475 |
LitVar | rs4538475 |
Map | rs4538475 |
PheGenI | rs4538475 |
Biobank | rs4538475 |
1000 genomes | rs4538475 |
hgdp | rs4538475 |
ensembl | rs4538475 |
geneview | rs4538475 |
scholar | rs4538475 |
rs4538475 | |
pharmgkb | rs4538475 |
gwascentral | rs4538475 |
openSNP | rs4538475 |
23andMe | rs4538475 |
SNPshot | rs4538475 |
SNPdbe | rs4538475 |
MSV3d | rs4538475 |
GWAS Ctlg | rs4538475 |
GMAF | 0.3127 |
Max Magnitude | 2 |
? | (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] |