rs61732609
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs61732609(C;C) |
| Make rs61732609(C;T) |
| Make rs61732609(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 42627674 |
| Gene | CYB5R3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61732609 |
| dbSNP (classic) | rs61732609 |
| ClinGen | rs61732609 |
| ebi | rs61732609 |
| HLI | rs61732609 |
| Exac | rs61732609 |
| Gnomad | rs61732609 |
| Varsome | rs61732609 |
| LitVar | rs61732609 |
| Map | rs61732609 |
| PheGenI | rs61732609 |
| Biobank | rs61732609 |
| 1000 genomes | rs61732609 |
| hgdp | rs61732609 |
| ensembl | rs61732609 |
| geneview | rs61732609 |
| scholar | rs61732609 |
| rs61732609 | |
| pharmgkb | rs61732609 |
| gwascentral | rs61732609 |
| openSNP | rs61732609 |
| 23andMe | rs61732609 |
| SNPshot | rs61732609 |
| SNPdbe | rs61732609 |
| MSV3d | rs61732609 |
| GWAS Ctlg | rs61732609 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs61732609(A;A) |
| Alt | rs61732609(A;A) |
| Reference | Rs61732609(G;G) |
| Significance | Pathogenic |
| Disease | Methemoglobinemia type 2 |
| Variation | info |
| Gene | CYB5R3 |
| CLNDBN | Methemoglobinemia type 2 |
| Reversed | 0 |
| HGVS | NC_000022.10:g.43023680G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000000272.3, |
