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| Acute rhabdomyolysis v0.6 | SLC22A12 | Arina Puzriakova commented on gene: SLC22A12: After NHS Genomic Medicine Service consideration, the rating of this gene has been left as Red but may be subject to review in the future. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Acute rhabdomyolysis v0.3 | SLC22A12 | Arina Puzriakova reviewed gene: SLC22A12: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Hypouricemia, renal, OMIM:220150; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Acute rhabdomyolysis v0.2 | SLC22A12 |
Arina Puzriakova gene: SLC22A12 was added gene: SLC22A12 was added to Acute rhabdomyolysis. Sources: Expert Review Red,NHS GMS Mode of inheritance for gene: SLC22A12 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SLC22A12 were set to Exercise induced acute kidney failure; Hypouricemia, renal, OMIM:220150 |
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