Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9863
Gene Symbol: MAGI2
MAGI2
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		0.300 Biomarker GENOMICS_ENGLAND MAGI2 Mutations Cause Congenital Nephrotic Syndrome. 27932480

2017