| ? | (C;C) (C;T) (T;T) | 28 |
|---|
 |
[PMID 19430483]
23andMe blog blood pressure
| GWAS snp
|
| PMID
|
[PMID 21572416]
|
| Trait
|
|
| Title
|
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.
|
| Risk Allele
|
T
|
| P-val
|
4E-17
|
| Odds Ratio
|
1.1800 [0.91-1.45] mm Hg increase
|
[PMID 21963141] Genetic variations in CYP17A1, CACNB2 and PLEKHA7 are associated with blood pressure and/or hypertension in she ethnic minority of China
| GWAS snp
|
| PMID
|
[PMID 21909115]
|
| Trait
|
|
| Title
|
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|
| Risk Allele
|
T
|
| P-val
|
7E-26
|
| Odds Ratio
|
1.0950 [NR] mmHg increase
|
| GWAS snp
|
| PMID
|
[PMID 21909110]
|
| Trait
|
|
| Title
|
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|
| Risk Allele
|
T
|
| P-val
|
8E-11
|
| Odds Ratio
|
0.5290 [0.37-0.69] mmHg increase
|
[PMID 20852445] Common variants in or near FGF5, CYP17A1 and MTHFR genes are associated with blood pressure and hypertension in Chinese Hans.
[PMID 22504314] Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
[PMID 22525200] Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
| GET Evidence
|
| rs11191548
|
| aa_change
|
|
| aa_change_short
|
|
| impact
|
pathogenic
|
| qualified_impact
|
Insufficiently evaluated pathogenic
|
| overall_frequency
|
0.046875
|
| summary
|
|
[PMID 23133444] Genetic variation in CYP17A1 is associated with arterial stiffness in diabetic subjects
