MYRF, myelin regulatory factor, 745

N. diseases: 102; N. variants: 44
Disease: Scimitar Syndrome ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1565307564
rs1565307564 		0.807 0.120 11 61783599 missense variant A/G snv
CUI: C0036400
Disease: Scimitar Syndrome
Scimitar Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Cardiovascular Diseases 0.700 0