{{Rsnum
|rsid=228591
|Gene=ATM
|Chromosome=11
|position=108226606
|Orientation=plus
|GMAF=0.4757
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ATM
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 25.2 | 55.0 | 19.8
| HCB | 20.7 | 45.9 | 33.3
| JPT | 19.3 | 45.9 | 34.9
| YRI | 12.5 | 59.0 | 28.5
| ASW | 28.1 | 38.6 | 33.3
| CHB | 20.7 | 45.9 | 33.3
| CHD | 20.4 | 51.9 | 27.8
| GIH | 50.0 | 40.8 | 9.2
| LWK | 10.0 | 43.6 | 46.4
| MEX | 35.1 | 42.1 | 22.8
| MKK | 10.5 | 43.1 | 46.4
| TSI | 54.1 | 34.7 | 11.2
| HapMapRevision=28
}}

{{PMID|18451257}} [[rs8178085]] and [[rs12334811]] with approaching dose-dependent effect on [[lung cancer]] predisposition, subjects carrying two to four risk genotypes were associated with a 43% decreased lung cancer risk compared with subjects carrying zero to one risk genotypes (adjusted odds ratio, 0.53; 95% confidence interval, 0.35-0.80).

[[rs228591]] variant allele or ataxia-telangiectasia and Rad3-related [[rs6782400]] wild-type homozygous genotype

{{PMID Auto
|PMID=16091150
|Title=Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes.
|OA=1
}}

{{PMID Auto
|PMID=19276285
|Title=Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}