MAGEL2, MAGE family member L2, 54551

N. diseases: 184; N. variants: 15
Disease: Prader-Willi-like syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1566784441
rs1566784441
Entrez Id: 54551
Gene Symbol: MAGEL2
MAGEL2
CUI: C3809877
Disease:
Prader-Willi-like syndrome 		T 0.700 CausalMutation CLINVAR