rs118203396
A SNP in the TSC1 gene on chromosome 9. Its most notable genotype is A;G: Tuberous Sclerosis Complex
- Gene
- TSC1
- Location
- Chr 9132,921,943 (GRCh38)
- Highest magnitude
- 6.3Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- A;GMost notableBadTuberous Sclerosis Complex
- A;AGoodcommon in clinvar
SNPedia records rs118203396 on the minus strand: (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other TSC1 SNPs
- rs118203352G;TTuberous Sclerosis ComplexVery important
- rs118203360-;TCTuberous Sclerosis ComplexVery important
- rs118203387C;TTuberous Sclerosis ComplexVery important
- rs118203388G;TTuberous Sclerosis ComplexVery important
- rs118203402C;GTuberous Sclerosis ComplexVery important
- rs118203423C;GTuberous Sclerosis ComplexVery important
- rs118203426A;CTuberous Sclerosis ComplexVery important
- rs118203427A;GTuberous Sclerosis ComplexVery important
Notes
From SNPedia
Notes
Missense mutations to the TSC1 gene cause tuberous sclerosis complex.
Source and license
Adapted from rs118203396 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.