rs1763442
From SNPedia
| Merged into | rs1144520 |
| Orientation | plus |
| Make rs1763442(A;A) |
| Make rs1763442(A;T) |
| Make rs1763442(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 10 |
| Position | 29097084 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1763442 |
| dbSNP (classic) | rs1763442 |
| ClinGen | rs1763442 |
| ebi | rs1763442 |
| HLI | rs1763442 |
| Exac | rs1763442 |
| Gnomad | rs1763442 |
| Varsome | rs1763442 |
| LitVar | rs1763442 |
| Map | rs1763442 |
| PheGenI | rs1763442 |
| Biobank | rs1763442 |
| 1000 genomes | rs1763442 |
| hgdp | rs1763442 |
| ensembl | rs1763442 |
| geneview | rs1763442 |
| scholar | rs1763442 |
| rs1763442 | |
| pharmgkb | rs1763442 |
| gwascentral | rs1763442 |
| openSNP | rs1763442 |
| 23andMe | rs1763442 |
| SNPshot | rs1763442 |
| SNPdbe | rs1763442 |
| MSV3d | rs1763442 |
| GWAS Ctlg | rs1763442 |
| Status | Merged into rs1144520 |
| Max Magnitude | 0 |
The ferrochelatase FECH gene is involved in the metabolism of heme. Deficiencies of the enzyme can cause erythropoietic protoporphyria, a type of photosensitivity that can cause serious skin reactions.[1] This inherited condition has incomplete penetrance.
