{{Rsnum
|rsid=659243
|Gene=ATM
|Chromosome=11
|position=108312440
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|GMAF=0
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.9 | 99.1
| HCB | 0.0 | 0.8 | 99.2
| JPT | 0.0 | 2.7 | 97.3
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.8 | 99.2
| CHD | 0.0 | 0.9 | 99.1
| GIH | 0.0 | 1.0 | 99.0
| LWK | 0.0 | 1.8 | 98.2
| MEX | 0.0 | 5.3 | 94.7
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 1.0 | 99.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=659243
|allele=G
|frequency=1
|uid=1103649787059
|type=homozygous_SNP
|hugo=ATM
|ensembl gene=ENSG00000149311
|ensembl transcript=ENST00000278616
|sift=TOLERATED
|disease=Defects in ATM contribute to B-cell chronic lymphocytic leukemia (BCLL). BCLL is the commonest form of leukemia in the elderly. It is characterized by the accumulation of mature CD5+ B lymphocytes, lymphadenopathy, immunodeficiency and bone marrow failure.
}}

{{GET Evidence
|gene=ATM
|aa_change=Asn1983Ser
|aa_change_short=N1983S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs659243
|overall_frequency_n=128
|overall_frequency_d=128
|overall_frequency=1
|n_genomes=56
|n_genomes_annotated=0
|n_haplomes=112
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=3
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=0
|autoscore=3
|n_web_uneval=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}