rs419076
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs419076(C;C) |
| Make rs419076(C;T) |
| Make rs419076(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 169383098 |
| Gene | MECOM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs419076 |
| dbSNP (classic) | rs419076 |
| ClinGen | rs419076 |
| ebi | rs419076 |
| HLI | rs419076 |
| Exac | rs419076 |
| Gnomad | rs419076 |
| Varsome | rs419076 |
| LitVar | rs419076 |
| Map | rs419076 |
| PheGenI | rs419076 |
| Biobank | rs419076 |
| 1000 genomes | rs419076 |
| hgdp | rs419076 |
| ensembl | rs419076 |
| geneview | rs419076 |
| scholar | rs419076 |
| rs419076 | |
| pharmgkb | rs419076 |
| gwascentral | rs419076 |
| openSNP | rs419076 |
| 23andMe | rs419076 |
| SNPshot | rs419076 |
| SNPdbe | rs419076 |
| MSV3d | rs419076 |
| GWAS Ctlg | rs419076 |
| GMAF | 0.4164 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21909115 ]
|
| Trait | |
| Title | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. |
| Risk Allele | T |
| P-val | 2E-13 |
| Odds Ratio | 0.4090 [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-13 |
| Odds Ratio | 0.3400 [0.25-0.43] mmHg increase |
