rs119469012
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs119469012(G;G) |
| Make rs119469012(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 58272825 |
| Gene | MPO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs119469012 |
| dbSNP (classic) | rs119469012 |
| ClinGen | rs119469012 |
| ebi | rs119469012 |
| HLI | rs119469012 |
| Exac | rs119469012 |
| Gnomad | rs119469012 |
| Varsome | rs119469012 |
| LitVar | rs119469012 |
| Map | rs119469012 |
| PheGenI | rs119469012 |
| Biobank | rs119469012 |
| 1000 genomes | rs119469012 |
| hgdp | rs119469012 |
| ensembl | rs119469012 |
| geneview | rs119469012 |
| scholar | rs119469012 |
| rs119469012 | |
| pharmgkb | rs119469012 |
| gwascentral | rs119469012 |
| openSNP | rs119469012 |
| 23andMe | rs119469012 |
| SNPshot | rs119469012 |
| SNPdbe | rs119469012 |
| MSV3d | rs119469012 |
| GWAS Ctlg | rs119469012 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs119469012(G;G) |
| Alt | rs119469012(G;G) |
| Reference | Rs119469012(T;T) |
| Significance | Pathogenic |
| Disease | Myeloperoxidase deficiency |
| Variation | info |
| Gene | MPO |
| CLNDBN | Myeloperoxidase deficiency |
| Reversed | 1 |
| HGVS | NC_000017.10:g.56350186A>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000003815.3, |
