rs8178085
A SNP in the PRKDC gene on chromosome 8. Its most notable genotype is T;T: common in complete genomics
- Gene
- PRKDC
- Location
- Chr 847,898,144 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 3%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs8178085 on the minus strand: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 9 HapMap populations.
- AverageT;T 91%
- European ancestry (Utah)T;T 100%
- Han Chinese (Beijing)T;T 85%
- Japanese (Tokyo)T;T 91%
- Yoruba (Nigeria)T;T 91%
- African ancestry (Southwest US)T;T 93%
- Chinese (Denver)T;T 84%
- Gujarati IndianT;T 99%
- Luhya (Kenya)T;T 86%
- Maasai (Kenya)T;T 94%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
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
Source and license
Adapted from rs8178085 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.