Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909219
rs121909219
PTEN
T 0.700 CausalMutation CLINVAR

dbSNP: rs150766139
rs150766139
NTHL1 ; TSC2
A 0.700 CausalMutation CLINVAR

dbSNP: rs775248597
rs775248597
ATM
T 0.700 CausalMutation CLINVAR