rs997026784
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs997026784(C;C) |
| Make rs997026784(C;T) |
| Make rs997026784(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 17 |
| Position | 74862864 |
| Gene | FDXR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs997026784 |
| dbSNP (classic) | rs997026784 |
| ClinGen | rs997026784 |
| ebi | rs997026784 |
| HLI | rs997026784 |
| Exac | rs997026784 |
| Gnomad | rs997026784 |
| Varsome | rs997026784 |
| LitVar | rs997026784 |
| Map | rs997026784 |
| PheGenI | rs997026784 |
| Biobank | rs997026784 |
| 1000 genomes | rs997026784 |
| hgdp | rs997026784 |
| ensembl | rs997026784 |
| geneview | rs997026784 |
| scholar | rs997026784 |
| rs997026784 | |
| pharmgkb | rs997026784 |
| gwascentral | rs997026784 |
| openSNP | rs997026784 |
| 23andMe | rs997026784 |
| SNPshot | rs997026784 |
| SNPdbe | rs997026784 |
| MSV3d | rs997026784 |
| GWAS Ctlg | rs997026784 |
| Max Magnitude | 0 |
aka NM_024417.4(FDXR):c.1429G>A or (p.Glu477Lys)
OMIM pathogenic variant
