Gene: SMARCD2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6603
Gene Symbol: SMARCD2
SMARCD2 		0.400 Biomarker disease CTD_human Studying patients from three unrelated pedigrees characterized by neutropenia, specific granule deficiency, myelodysplasia with excess of blast cells, and various developmental aberrations, we identified three homozygous loss-of-function mutations in SMARCD2. 28369036 2017
Entrez Id: 6603
Gene Symbol: SMARCD2
SMARCD2 		0.400 Biomarker disease HPO