MAGEL2, MAGE family member L2, 54551

N. diseases: 184; N. variants: 15
Disease: Prader-Willi-like 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: rs1060499934
rs1060499934 		1.000 0.080 15 23644785 frameshift variant C/- delins
CUI: C3809877
Disease: Prader-Willi-like syndrome
Prader-Willi-like syndrome 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.700 0