rs17458018
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common genotype |
| Make rs17458018(C;C) |
| Make rs17458018(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 215420652 |
| Gene | FN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17458018 |
| dbSNP (classic) | rs17458018 |
| ClinGen | rs17458018 |
| ebi | rs17458018 |
| HLI | rs17458018 |
| Exac | rs17458018 |
| Gnomad | rs17458018 |
| Varsome | rs17458018 |
| LitVar | rs17458018 |
| Map | rs17458018 |
| PheGenI | rs17458018 |
| Biobank | rs17458018 |
| 1000 genomes | rs17458018 |
| hgdp | rs17458018 |
| ensembl | rs17458018 |
| geneview | rs17458018 |
| scholar | rs17458018 |
| rs17458018 | |
| pharmgkb | rs17458018 |
| gwascentral | rs17458018 |
| openSNP | rs17458018 |
| 23andMe | rs17458018 |
| SNPshot | rs17458018 |
| SNPdbe | rs17458018 |
| MSV3d | rs17458018 |
| GWAS Ctlg | rs17458018 |
| GMAF | 0.03352 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22319020 ]
|
| Trait | |
| Title | A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex. |
| Risk Allele | |
| P-val | 0.000007 |
| Odds Ratio | 1.2200 None |
