rs17115100
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common on affy axiom data |
(G;T) | 1.5 | slightly increased risk of developing Parkinson's Disease |
(T;T) | 2 | Increased risk of developing Parkinson's Disease |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 102831636 |
Gene | CYP17A1, CYP17A1-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs17115100 |
dbSNP (classic) | rs17115100 |
ClinGen | rs17115100 |
ebi | rs17115100 |
HLI | rs17115100 |
Exac | rs17115100 |
Gnomad | rs17115100 |
Varsome | rs17115100 |
LitVar | rs17115100 |
Map | rs17115100 |
PheGenI | rs17115100 |
Biobank | rs17115100 |
1000 genomes | rs17115100 |
hgdp | rs17115100 |
ensembl | rs17115100 |
geneview | rs17115100 |
scholar | rs17115100 |
rs17115100 | |
pharmgkb | rs17115100 |
gwascentral | rs17115100 |
openSNP | rs17115100 |
23andMe | rs17115100 |
SNPshot | rs17115100 |
SNPdbe | rs17115100 |
MSV3d | rs17115100 |
GWAS Ctlg | rs17115100 |
GMAF | 0.1593 |
Max Magnitude | 2 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19915575] |
Trait | Parkinson's disease |
Title | Genome-wide association study reveals genetic risk underlying Parkinson's disease |
Risk Allele | T |
P-val | 7E-8 |
Odds Ratio | 1.25 [NR] |
[PMID 26263970] A Single Nucleotide Polymorphism near the CYP17A1 Gene Is Associated with Left Ventricular Mass in Hypertensive Patients under Pharmacotherapy