rs104893811
A SNP in the TGFBR2 gene on chromosome 3. Its most notable genotype is C;T: Loeys-Dietz Syndrome
- Gene
- TGFBR2
- Location
- Chr 330,674,228 (GRCh38)
- Highest magnitude
- 7.0Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- C;TMost notableBadLoeys-Dietz Syndrome
On SNPedia: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other TGFBR2 SNPs
- rs28934568C;TLoeys-Dietz SyndromeVery important
- rs104893807C;GLoeys-Dietz SyndromeVery important
- rs104893809C;TLoeys-Dietz SyndromeVery important
- rs104893810C;TLoeys-Dietz SyndromeVery important
- rs104893812A;TLoeys-Dietz SyndromeVery important
- rs104893813C;GLoeys-Dietz SyndromeVery important
- rs104893814G;TLoeys-Dietz SyndromeVery important
- rs104893815A;GLoeys-Dietz SyndromeVery important
Source and license
Adapted from rs104893811 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.