MYRF, myelin regulatory factor, 745

N. diseases: 102; N. variants: 44
Disease: Congenital diaphragmatic hernia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1565286228
rs1565286228
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C0235833
Disease:
Congenital diaphragmatic hernia 		T 0.700 CausalMutation CLINVAR