Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1064793345
rs1064793345
C 0.700 GeneticVariation CLINVAR Lifetime cancer risks in individuals with germline PTEN mutations. 22252256

2012

dbSNP: rs1064793345
rs1064793345
C 0.700 GeneticVariation CLINVAR Estimate of de novo mutation frequency in probands with PTEN hamartoma tumor syndrome. 22595938

2012

dbSNP: rs1085308039
rs1085308039
T 0.700 CausalMutation CLINVAR

dbSNP: rs1085308040
rs1085308040
A 0.700 CausalMutation CLINVAR

dbSNP: rs1085308041
rs1085308041
G 0.700 CausalMutation CLINVAR

dbSNP: rs1085308042
rs1085308042
A 0.700 CausalMutation CLINVAR

dbSNP: rs1085308043
rs1085308043
G 0.700 CausalMutation CLINVAR

dbSNP: rs1085308044
rs1085308044
C 0.700 CausalMutation CLINVAR

dbSNP: rs1085308045
rs1085308045
G 0.700 CausalMutation CLINVAR

dbSNP: rs1085308046
rs1085308046
C 0.700 CausalMutation CLINVAR

dbSNP: rs1085308047
rs1085308047
G 0.700 CausalMutation CLINVAR

dbSNP: rs1085308048
rs1085308048
G 0.700 CausalMutation CLINVAR

dbSNP: rs1085308049
rs1085308049
T 0.700 CausalMutation CLINVAR

dbSNP: rs1085308050
rs1085308050
TA 0.700 CausalMutation CLINVAR

dbSNP: rs1085308051
rs1085308051
G 0.700 CausalMutation CLINVAR

dbSNP: rs1085308052
rs1085308052
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1085308053
rs1085308053
T 0.700 CausalMutation CLINVAR

dbSNP: rs1085308054
rs1085308054
C 0.700 CausalMutation CLINVAR

dbSNP: rs1085308055
rs1085308055
T 0.700 CausalMutation CLINVAR

dbSNP: rs1085308056
rs1085308056
G 0.700 CausalMutation CLINVAR

dbSNP: rs121909218
rs121909218
A 0.700 CausalMutation CLINVAR

dbSNP: rs121909219
rs121909219
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909224
rs121909224
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909231
rs121909231
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913293
rs121913293
T 0.700 CausalMutation CLINVAR