rs664143
A SNP in the ATM gene on chromosome 11. Its most notable genotype is A;G: Higher risk for number of cancers
- Gene
- ATM
- Location
- Chr 11108,354,934 (GRCh38)
- Highest magnitude
- 2.5Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 40%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GNot ratednormal
- A;GMost notableBadHigher risk for number of cancers
- A;ABadHigher risk for number of cancers
SNPedia records rs664143 on the minus strand: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageG;G 37% A;G 44% A;A 19%
- European ancestry (Utah)G;G 27% A;G 54% A;A 19%
- Han Chinese (Beijing)G;G 23% A;G 44% A;A 34%
- Japanese (Tokyo)G;G 24% A;G 42% A;A 35%
- Yoruba (Nigeria)G;G 46% A;G 48% A;A 6%
- African ancestry (Southwest US)G;G 56% A;G 30% A;A 14%
- Chinese (Denver)G;G 21% A;G 51% A;A 28%
- Gujarati IndianG;G 52% A;G 39% A;A 10%
- Luhya (Kenya)G;G 41% A;G 47% A;A 12%
- Mexican ancestry (Los Angeles)G;G 38% A;G 41% A;A 21%
- Maasai (Kenya)G;G 27% A;G 50% A;A 23%
- TuscanG;G 55% A;G 33% A;A 12%
Related
Conditions, medicines and genes
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
Show notes, about 150 words
600+ Korean lung cancer patients were part of a study that concluded that the rs664143(T) allele, as oriented vis-a-vis dbSNP, located in the ATM gene and also known as IVS62+60G>A, was associated with increased risk, with an odds ratio of 1.68 (CI: 1.1-2.1, p<0.05). In a study of 119 American patients with potentially resectable pancreatic cancer, the rs664143(C) allele was associated with poorer overall survival (ie response) to combined gerncitabine radiation therapy. Also, as 1 of 3 SNPs its risk allele is associated with poorer overall survival for pancreatic cancer patients being treated with combined gerncitabine radiation therapy; median overall survival times of 31.0, 16.2, and 10.5 months were calculated for pancreatic cancer patients carrying < or = 1, 2, and 3 risk alleles from rs664143(C), rs2227928(C), and rs521102(T;T), respectively (P=0.004).
Source and license
Adapted from rs664143 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.