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MYH9 and leukemia are reported together in 1 article.
Gene
MYH9
- HGNC
- HGNC:7579
6articles
6mentions
4variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
Phenotype
Leukemia
652articles
652mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60Utility of next-generation sequencing technologies for the efficient genetic resolution of haematological disorders.
PMID 25703294 | DOI 10.1111/cge.12573 · Clinical genetics · 2016 · 6 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MYH9 | “The final two cases (MYH9 associated macrothrombocytopenia associated with multiple congenital anomalies; atypical juvenile myelomonocytic leukaemia associated with a KRAS mutation) highlight the utility of NGS where the diagnosis is less certain, or where there is an unusual phenotype.” | 0.98 | hgnc_dict_v1 |
| phenotype | leukemia | “The final two cases (MYH9 associated macrothrombocytopenia associated with multiple congenital anomalies; atypical juvenile myelomonocytic leukaemia associated with a KRAS mutation) highlight the utility of NGS where the diagnosis is less certain, or where there is an unusual phenotype.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | RPS19 | “Mutations in RPS19, ELANE and FANCD2 were found.” | 0.98 | hgnc_dict_v1 |
| gene | ELANE | “Mutations in RPS19, ELANE and FANCD2 were found.” | 0.98 | hgnc_dict_v1 |