rs5943057
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5943057(G;G) |
| Make rs5943057(G;T) |
| Make rs5943057(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 110695977 |
| Gene | CHRDL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5943057 |
| dbSNP (classic) | rs5943057 |
| ClinGen | rs5943057 |
| ebi | rs5943057 |
| HLI | rs5943057 |
| Exac | rs5943057 |
| Gnomad | rs5943057 |
| Varsome | rs5943057 |
| LitVar | rs5943057 |
| Map | rs5943057 |
| PheGenI | rs5943057 |
| Biobank | rs5943057 |
| 1000 genomes | rs5943057 |
| hgdp | rs5943057 |
| ensembl | rs5943057 |
| geneview | rs5943057 |
| scholar | rs5943057 |
| rs5943057 | |
| pharmgkb | rs5943057 |
| gwascentral | rs5943057 |
| openSNP | rs5943057 |
| 23andMe | rs5943057 |
| SNPshot | rs5943057 |
| SNPdbe | rs5943057 |
| MSV3d | rs5943057 |
| GWAS Ctlg | rs5943057 |
| GMAF | 0.3718 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21378988] |
| Trait | |
| Title | A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease |
| Risk Allele | |
| P-val | 9E-7 |
| Odds Ratio | None None |
