rs8110090
A SNP in the TGFB1 gene on chromosome 19. Its most notable genotype is A;A: common in complete genomics
- Gene
- TGFB1
- Location
- Chr 1941,339,967 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 6%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). 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.
- AverageA;A 82%
- European ancestry (Utah)A;A 92%
- Han Chinese (Beijing)A;A 97%
- Japanese (Tokyo)A;A 100%
- Yoruba (Nigeria)A;A 71%
- African ancestry (Southwest US)A;A 73%
- Chinese (Denver)A;A 99%
- Gujarati IndianA;A 66%
- Luhya (Kenya)A;A 67%
- Mexican ancestry (Los Angeles)A;A 78%
- Maasai (Kenya)A;A 72%
- TuscanA;A 84%
Related
Other TGFB1 SNPs
- rs1800469G;Glower TGF-β1 levels, higher risk for COPD?Minor
- rs1800470A;GNo summary available.Typical
- rs1800471C;Ccommon in clinvarTypical
- rs1800472G;Gcommon on affy axiom dataTypical
- rs1982073G;Grisk genotype for several disordersTypical
- rs2241715A;Acommon in clinvarTypical
- rs4803455C;Ccommon in clinvarTypical
- rs8179181G;Gcommon in clinvarTypical
Source and license
Adapted from rs8110090 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.