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| COVID-19 research v0.180 | SMARCD2 | Sophie Hambleton reviewed gene: SMARCD2: Rating: GREEN; Mode of pathogenicity: None; Publications: 28369036; Phenotypes: neutropenia, specific granule deficiency, myelodysplasia, developmental delay, dysmorphic features; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| COVID-19 research v0.40 | SMARCD2 |
Ellen McDonagh Source Expert Review Green was added to SMARCD2. Added phenotypes Congenital defects of phagocyte number or function; Neutropenia, developmental aberrations, skeletal abnormalities, hematopoietic stem cells, myelodysplasia for gene: SMARCD2 Rating Changed from Red List (low evidence) to Green List (high evidence) |
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| COVID-19 research v0.36 | SMARCD2 |
Ellen McDonagh gene: SMARCD2 was added gene: SMARCD2 was added to Viral susceptibility. Sources: IUIS Classification February 2018,IUIS Classification December 2019 Mode of inheritance for gene: SMARCD2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SMARCD2 were set to 32086639; 32048120 Phenotypes for gene: SMARCD2 were set to Congenital defects of phagocyte number or function; Neutropenia, developmental aberrations, skeletal abnormalities, hematopoietic stem cells, myelodysplasia |
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