rs397514871
A SNP in the TSC1 gene on chromosome 9. Its most notable genotype is A;G: Tuberous Sclerosis Complex
- Gene
- TSC1
- Location
- Chr 9132,897,538 (GRCh38)
- Highest magnitude
- 6.3Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- A;GMost notableBadTuberous Sclerosis Complex
SNPedia records rs397514871 on the minus strand: (C;C), (C;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
- rs118203396A;GTuberous Sclerosis ComplexVery important
- rs118203402C;GTuberous Sclerosis ComplexVery important
- rs118203423C;GTuberous Sclerosis ComplexVery important
- rs118203426A;CTuberous Sclerosis ComplexVery important
Source and license
Adapted from rs397514871 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.