rs3096277
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3096277(C;C) |
| Make rs3096277(C;T) |
| Make rs3096277(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 83730599 |
| Gene | CDH13, LOC105371366 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3096277 |
| dbSNP (classic) | rs3096277 |
| ClinGen | rs3096277 |
| ebi | rs3096277 |
| HLI | rs3096277 |
| Exac | rs3096277 |
| Gnomad | rs3096277 |
| Varsome | rs3096277 |
| LitVar | rs3096277 |
| Map | rs3096277 |
| PheGenI | rs3096277 |
| Biobank | rs3096277 |
| 1000 genomes | rs3096277 |
| hgdp | rs3096277 |
| ensembl | rs3096277 |
| geneview | rs3096277 |
| scholar | rs3096277 |
| rs3096277 | |
| pharmgkb | rs3096277 |
| gwascentral | rs3096277 |
| openSNP | rs3096277 |
| 23andMe | rs3096277 |
| SNPshot | rs3096277 |
| SNPdbe | rs3096277 |
| MSV3d | rs3096277 |
| GWAS Ctlg | rs3096277 |
| GMAF | 0.3136 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 17903302 ]
|
| Trait | Blood pressure |
| Title | Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness |
| Risk Allele | |
| P-val | 1.0000000000000001E-9 |
| Odds Ratio | NR NR |
[PMID 19304780] Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations.
[PMID 19439027] Dissecting complex traits: recent advances in hypertension genomics.
[PMID 27682011] The T>A (rs11646213) gene polymorphism of cadherin-13 (CDH13) gene is associated with decreased risk of developing hypertension in Mexican population.
