rs863223501
A SNP in the COL5A2 gene on chromosome 2. Its most notable genotype is C;T: Ehlers-Danlos Syndrome (EDS) classic type
- Gene
- COL5A2
- Location
- Chr 2189,104,271 (GRCh38)
- Highest magnitude
- 5.5Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;TMost notableBadEhlers-Danlos Syndrome (EDS) classic type
- C;CGoodcommon in clinvar
SNPedia records rs863223501 on the minus strand: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other COL5A2 SNPs
- rs121912930C;GEhlers-Danlos Syndrome (EDS) classic typeVery important
- rs770598613C;GEhlers-Danlos Syndrome (EDS) classic typeVery important
- rs786205103-;AGGGAGCEhlers-Danlos Syndrome (EDS) classic typeVery important
- rs786205104A;CEhlers-Danlos Syndrome (EDS) classic typeVery important
- rs878853978C;TEhlers-Danlos Syndrome (EDS) classic typeVery important
Source and license
Adapted from rs863223501 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.