rs1004467
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 |
| Make rs1004467(C;C) |
| Make rs1004467(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 102834750 |
| Gene | CYP17A1, CYP17A1-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1004467 |
| dbSNP (classic) | rs1004467 |
| ClinGen | rs1004467 |
| ebi | rs1004467 |
| HLI | rs1004467 |
| Exac | rs1004467 |
| Gnomad | rs1004467 |
| Varsome | rs1004467 |
| LitVar | rs1004467 |
| Map | rs1004467 |
| PheGenI | rs1004467 |
| Biobank | rs1004467 |
| 1000 genomes | rs1004467 |
| hgdp | rs1004467 |
| ensembl | rs1004467 |
| geneview | rs1004467 |
| scholar | rs1004467 |
| rs1004467 | |
| pharmgkb | rs1004467 |
| gwascentral | rs1004467 |
| openSNP | rs1004467 |
| 23andMe | rs1004467 |
| SNPshot | rs1004467 |
| SNPdbe | rs1004467 |
| MSV3d | rs1004467 |
| GWAS Ctlg | rs1004467 |
| GMAF | 0.1993 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19430479 ]
|
| Trait | Systolic blood pressure |
| Title | Genome-wide association study of blood pressure and hypertension |
| Risk Allele | A |
| P-val | 1E-10 |
| Odds Ratio | 1.05 [0.74-1.36] mm Hg increase |
[PMID 20921432] Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension. The Japanese Millennium Genome Project
[PMID 20852445] Common variants in or near FGF5, CYP17A1 and MTHFR genes are associated with blood pressure and hypertension in Chinese Hans.
[PMID 23133444] Genetic variation in CYP17A1 is associated with arterial stiffness in diabetic subjects
[PMID 22714708] Genetic polymorphisms of CYP17A1 in steroidogenesis pathway are associated with risk of progression to castration-resistant prostate cancer in Japanese men receiving androgen deprivation therapy.
[PMID 23102448] Physical activity modifies the associations between genetic variants and hypertension in the Chinese children.
[PMID 23591986] Influence of obesity on association between genetic variants identified by genome-wide association studies and hypertension risk in Chinese children.
[PMID 24671014] Genetic risk assessment for cardiovascular disease with seven genes associated with plasma C-reactive protein concentrations in Asian populations
[PMID 25917616] CYP17A1 and CYP2E1 Variants Associated with High Altitude Polycythemia in Tibetans at the Qinghai-Tibetan Plateau
[PMID 25990650] The relationship between the polymorphisms of the CYP17A1 gene and hypertension: A meta-analysis
[PMID 26263970] A Single Nucleotide Polymorphism near the CYP17A1 Gene Is Associated with Left Ventricular Mass in Hypertensive Patients under Pharmacotherapy
[PMID 32185238] Haplotype Analysis of Candidate Genes Involved in Inflammation and Oxidative Stress and the Susceptibility to Preeclampsia.
