Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909224
rs121909224
G 0.700 CausalMutation CLINVAR The PI3K pathway as drug target in human cancer. 20085938

2010

dbSNP: rs121909224
rs121909224
T 0.700 CausalMutation CLINVAR The PI3K pathway as drug target in human cancer. 20085938

2010

dbSNP: rs121909229
rs121909229
A 0.700 CausalMutation CLINVAR The PI3K pathway as drug target in human cancer. 20085938

2010

dbSNP: rs121909224
rs121909224
T 0.700 CausalMutation CLINVAR PTEN and the PI3-kinase pathway in cancer. 18767981

2009

dbSNP: rs121909224
rs121909224
G 0.700 CausalMutation CLINVAR PTEN and the PI3-kinase pathway in cancer. 18767981

2009

dbSNP: rs121909229
rs121909229
A 0.700 CausalMutation CLINVAR PTEN and the PI3-kinase pathway in cancer. 18767981

2009

dbSNP: rs121909224
rs121909224
T 0.700 CausalMutation CLINVAR Enhanced sensitivity of PTEN-deficient tumors to inhibition of FRAP/mTOR. 11504908

2001

dbSNP: rs121909224
rs121909224
G 0.700 CausalMutation CLINVAR Enhanced sensitivity of PTEN-deficient tumors to inhibition of FRAP/mTOR. 11504908

2001

dbSNP: rs121909229
rs121909229
A 0.700 CausalMutation CLINVAR Enhanced sensitivity of PTEN-deficient tumors to inhibition of FRAP/mTOR. 11504908

2001

dbSNP: rs1057517809
rs1057517809
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519368
rs1057519368
G 0.700 CausalMutation CLINVAR

dbSNP: rs121909219
rs121909219
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909229
rs121909229
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121909231
rs121909231
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913294
rs121913294
T 0.700 GeneticVariation CLINVAR

dbSNP: rs146650273
rs146650273
G 0.700 CausalMutation CLINVAR

dbSNP: rs1564566861
rs1564566861
C 0.700 CausalMutation CLINVAR

dbSNP: rs1564570283
rs1564570283
C 0.700 CausalMutation CLINVAR

dbSNP: rs1564801750
rs1564801750
AG 0.700 CausalMutation CLINVAR

dbSNP: rs1564814454
rs1564814454
C 0.700 CausalMutation CLINVAR

dbSNP: rs1564826829
rs1564826829
0.700 CausalMutation CLINVAR

dbSNP: rs1564830444
rs1564830444
ATT 0.700 CausalMutation CLINVAR

dbSNP: rs1564838034
rs1564838034
C 0.700 CausalMutation CLINVAR

dbSNP: rs398123316
rs398123316
G 0.700 GeneticVariation CLINVAR

dbSNP: rs398123318
rs398123318
T 0.700 GeneticVariation CLINVAR