Rs11646213
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11646213 |
| PheGenI | rs11646213 |
| nextbio | rs11646213 |
| hapmap | rs11646213 |
| 1000 genomes | rs11646213 |
| hgdp | rs11646213 |
| ensembl | rs11646213 |
| gopubmed | rs11646213 |
| geneview | rs11646213 |
| scholar | rs11646213 |
| rs11646213 | |
| pharmgkb | rs11646213 |
| gwascentral | rs11646213 |
| openSNP | rs11646213 |
| 23andMe | rs11646213 |
| 23andMe all | rs11646213 |
| SNP Nexus | |
| SNPshot | rs11646213 |
| SNPdbe | rs11646213 |
| MSV3d | rs11646213 |
| Chromosome | 16 |
| Orientation | plus |
| GMAF | 0.3668 |
| Position | 82642651 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs11646213(A;A) |
| Make rs11646213(A;T) |
| Make rs11646213(T;T) |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
| GWAS snp | |
|---|---|
| PMID | [PMID 19304780] |
| Trait | Hypertension |
| Title | Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations |
| Risk Allele | T |
| P-val | 0.000008 |
| Odds Ratio | 1.28 [1.15-1.43] |
[PMID 19439027] Dissecting complex traits: recent advances in hypertension genomics.
[PMID 21872196] A variant upstream of the CDH13 adiponectin receptor gene and metabolic syndrome in Swedes.
| GET Evidence | |
|---|---|
| rs11646213 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.34375 |
| summary | |
