rs104894303
A SNP in the SDHD gene on chromosome 11. Its most notable genotype is C;T: Hereditary PGL/PCC Syndrome
- Gene
- SDHD
- Location
- Chr 11112,087,910 (GRCh38)
- Highest magnitude
- 6.2Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- C;TMost notableBadHereditary PGL/PCC 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 SDHD SNPs
- rs80338842A;GHereditary PGL/PCC SyndromeVery important
- rs80338843C;THereditary PGL/PCC SyndromeVery important
- rs80338844C;THereditary PGL/PCC SyndromeVery important
- rs80338845G;THereditary PGL/PCC SyndromeVery important
- rs80338847C;THereditary PGL/PCC SyndromeVery important
- rs104894302A;THereditary PGL/PCC SyndromeVery important
- rs104894304A;GHereditary PGL/PCC SyndromeVery important
- rs104894305A;CHereditary PGL/PCC SyndromeVery important
Source and license
Adapted from rs104894303 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.