rs80338764
A SNP in the LOC101448202 gene on chromosome 9. Its most notable genotype is C;G: Ehlers-Danlos Syndrome (EDS) classic type
- Gene
- LOC101448202
- Location
- Chr 9134,824,817 (GRCh38)
- Highest magnitude
- 5.5Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;GMost notableBadEhlers-Danlos Syndrome (EDS) classic type
- G;GGoodcommon in clinvar
On SNPedia: (C;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Source and license
Adapted from rs80338764 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.