rs752143061
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs752143061(A;A) |
| Make rs752143061(A;G) |
| Make rs752143061(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 17 |
| Position | 74864234 |
| Gene | FDXR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs752143061 |
| dbSNP (classic) | rs752143061 |
| ClinGen | rs752143061 |
| ebi | rs752143061 |
| HLI | rs752143061 |
| Exac | rs752143061 |
| Gnomad | rs752143061 |
| Varsome | rs752143061 |
| LitVar | rs752143061 |
| Map | rs752143061 |
| PheGenI | rs752143061 |
| Biobank | rs752143061 |
| 1000 genomes | rs752143061 |
| hgdp | rs752143061 |
| ensembl | rs752143061 |
| geneview | rs752143061 |
| scholar | rs752143061 |
| rs752143061 | |
| pharmgkb | rs752143061 |
| gwascentral | rs752143061 |
| openSNP | rs752143061 |
| 23andMe | rs752143061 |
| SNPshot | rs752143061 |
| SNPdbe | rs752143061 |
| MSV3d | rs752143061 |
| GWAS Ctlg | rs752143061 |
| Max Magnitude | 0 |
aka NM_024417.4(FDXR):c.916C>T or (p.Arg306Cys)
OMIM pathogenic variant
