rs373842615
A SNP in the ENG gene on chromosome 9. Its most notable genotype is C;T: Hereditary hemorrhagic telangiectasia
- Gene
- ENG
- Location
- Chr 9127,819,662 (GRCh38)
- Highest magnitude
- 4.3Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;TMost notableBadHereditary hemorrhagic telangiectasia
- T;TGoodcommon in clinvar
On SNPedia: (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other ENG SNPs
- rs121918401A;CHereditary hemorrhagic telangiectasiaVery important
- rs267606783A;GNo summary available.Very important
- rs863223539A;THereditary hemorrhagic telangiectasiaVery important
- rs863223542C;THereditary hemorrhagic telangiectasiaVery important
- rs863223543A;THereditary hemorrhagic telangiectasiaVery important
- rs11545664C;Ccommon in clinvarTypical
Source and license
Adapted from rs373842615 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.