rs730880096
A SNP in the LOC105379841 gene on chromosome 9. Its most notable genotype is A;G: Hereditary hemorrhagic telangiectasia
- Gene
- LOC105379841
- Location
- Chr 9127,829,788 (GRCh38)
- Highest magnitude
- 4.3Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- A;GMost notableBadHereditary hemorrhagic telangiectasia
SNPedia records rs730880096 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 LOC105379841 SNPs
- rs121918400G;THereditary hemorrhagic telangiectasiaVery important
- rs121918402G;THereditary hemorrhagic telangiectasiaVery important
- rs863223532A;GHereditary hemorrhagic telangiectasiaVery important
- rs863223537A;GHereditary hemorrhagic telangiectasiaVery important
- rs863223540-;GACAHereditary hemorrhagic telangiectasiaVery important
- rs864622666-;GGCCHereditary hemorrhagic telangiectasiaVery important
- rs878853657C;GHereditary hemorrhagic telangiectasiaVery important
Source and license
Adapted from rs730880096 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.