rs773920155
A SNP in the TSC2 gene on chromosome 16. Its most notable genotype is G;T: Tuberous Sclerosis Complex
- Gene
- TSC2
- Location
- Chr 162,061,946 (GRCh38)
- Highest magnitude
- 6.3Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- G;TMost notableBadTuberous Sclerosis Complex
On SNPedia: (G;G), (G;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other TSC2 SNPs
- rs28934872A;GTuberous Sclerosis ComplexVery important
- rs45438205C;TTuberous Sclerosis ComplexVery important
- rs45448101C;TTuberous Sclerosis ComplexVery important
- rs45451497C;TTuberous Sclerosis ComplexVery important
- rs45455296C;TTuberous Sclerosis ComplexVery important
- rs45462194A;GTuberous Sclerosis ComplexVery important
- rs45465195C;TTuberous Sclerosis ComplexVery important
- rs45466296A;GTuberous Sclerosis ComplexVery important
Source and license
Adapted from rs773920155 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.