rs6539267
A SNP in the POLR3B gene on chromosome 12. Its most notable genotype is C;C: normal
- Gene
- POLR3B
- Location
- Chr 12106,391,776 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 17%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableNot ratednormal
- C;TGood0.79x risk of Tourette's syndrome
- T;TGood0.79x risk of Tourette's syndrome
On SNPedia: (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.
- AverageC;C 4% C;T 24% T;T 72%
- European ancestry (Utah)C;C 12% C;T 32% T;T 57%
- Han Chinese (Beijing)C;C 0% C;T 10% T;T 90%
- Japanese (Tokyo)C;C 0% C;T 13% T;T 88%
- Yoruba (Nigeria)C;C <1% C;T 19% T;T 81%
- African ancestry (Southwest US)C;C 2% C;T 25% T;T 74%
- Chinese (Denver)C;C 0% C;T 12% T;T 88%
- Gujarati IndianC;C 13% C;T 36% T;T 52%
- Luhya (Kenya)C;C 0% C;T 16% T;T 84%
- Mexican ancestry (Los Angeles)C;C 2% C;T 32% T;T 67%
- Maasai (Kenya)C;C 1% C;T 35% T;T 64%
- TuscanC;C 11% C;T 38% T;T 52%
Related
Source and license
Adapted from rs6539267 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.