Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1085308040
rs1085308040
PTEN
CUI: C0036572
Disease: Seizures
Seizures 		A 0.700 CausalMutation CLINVAR

dbSNP: rs876660634
rs876660634
PTEN
CUI: C0036572
Disease: Seizures
Seizures 		G 0.700 CausalMutation CLINVAR