Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204433
rs786204433
ATM
T 0.700 CausalMutation CLINVAR ATM gene mutations in sporadic breast cancer patients from Brazil. 25625042

2015

dbSNP: rs786204433
rs786204433
ATM
T 0.700 CausalMutation CLINVAR Molecular defects in Moroccan patients with ataxia-telangiectasia. 23322442

2013

dbSNP: rs786204433
rs786204433
ATM
T 0.700 GeneticVariation CLINVAR Molecular defects in Moroccan patients with ataxia-telangiectasia. 23322442

2013

dbSNP: rs786204433
rs786204433
ATM
T 0.700 CausalMutation CLINVAR Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype. 21665257

2011

dbSNP: rs786204433
rs786204433
ATM
T 0.700 GeneticVariation CLINVAR Germline ATM mutational analysis in BRCA1/BRCA2 negative hereditary breast cancer families by MALDI-TOF mass spectrometry. 21445571

2011

dbSNP: rs786204433
rs786204433
ATM
T 0.700 GeneticVariation CLINVAR Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype. 21665257

2011

dbSNP: rs786204433
rs786204433
ATM
T 0.700 GeneticVariation CLINVAR Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: seven new mutations. 15039971

2004

dbSNP: rs786204433
rs786204433
ATM
T 0.700 CausalMutation CLINVAR Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: seven new mutations. 15039971

2004

dbSNP: rs786204433
rs786204433
ATM
T 0.700 GeneticVariation CLINVAR Independent mutational events are rare in the ATM gene: haplotype prescreening enhances mutation detection rate. 12815592

2003

dbSNP: rs786204433
rs786204433
ATM
T 0.700 CausalMutation CLINVAR Comprehensive scanning of the ATM gene with DOVAM-S. 12552559

2003

dbSNP: rs786204433
rs786204433
ATM
T 0.700 GeneticVariation CLINVAR Comprehensive scanning of the ATM gene with DOVAM-S. 12552559

2003

dbSNP: rs786204433
rs786204433
ATM
T 0.700 CausalMutation CLINVAR Independent mutational events are rare in the ATM gene: haplotype prescreening enhances mutation detection rate. 12815592

2003