Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs770374710
rs770374710
MAGEL2
CUI: C3809877
Disease: Prader-Willi-like syndrome
Prader-Willi-like syndrome 		TG 0.700 CausalMutation CLINVAR

dbSNP: rs770374710
rs770374710
MAGEL2
CUI: C3809877
Disease: Prader-Willi-like syndrome
Prader-Willi-like syndrome 		T 0.700 CausalMutation CLINVAR