rs786202800
A SNP in the ATM gene on chromosome 11. Its most notable genotype is -;TTTCAGTGCC: linked to certain hereditary cancers
- Gene
- ATM
- Location
- Chr 11108,343,348 (GRCh38)
- Highest magnitude
- 4.0Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- -;TTTCAGTGCCMost notableBadlinked to certain hereditary cancers
- TTTCAGTGCC;TTTCAGTGCCGoodcommon in clinvar
On SNPedia: (-;TTTCAGTGCC), (TTTCAGTGCC;TTTCAGTGCC). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other ATM SNPs
- rs147557621G;TBreast cancer associated mutationVery important
- rs200976093C;TBreast cancer associated mutationVery important
- rs376170600C;GBreast cancer associated mutationVery important
- rs376603775C;TBreast cancer associated mutationVery important
- rs529296539C;GBreast cancer associated mutationVery important
- rs587776551A;GBreast cancer associated mutationVery important
- rs587778080C;TBreast cancer associated mutationVery important
- rs587779813A;GBreast cancer associated mutationVery important
Notes
From SNPedia
Notes
-;TTTCAGTGCC
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer
References
Source and license
Adapted from rs786202800 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.