Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800057
rs1800057
ATM
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
G 0.730 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016

2018

dbSNP: rs1800057
rs1800057
ATM
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.730 GeneticVariation BEFREE A missense variant in ATM, rs1800057, associated with increased prostate cancer risk, was found exclusively in two high toxicity patients but did not reach statistical significance for association with radiosensitivity (P = 0.488). 19638463

2009

dbSNP: rs1800057
rs1800057
ATM
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.730 GeneticVariation BEFREE The ATM missense variant P1054R confers an about twofold increased risk for prostate cancer in our series. 17502119

2007

dbSNP: rs1800057
rs1800057
ATM
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.730 GeneticVariation BEFREE These results provide evidence that the presence of common variants in the ATM gene, may confer an altered cellular phenotype, and that the ATM 3161C>G variant might be associated with prostate cancer risk. 15280931

2004