rs771328239
A SNP in the SDHA gene on chromosome 5. Its most notable genotype is C;T: Hereditary PGL/PCC Syndrome
- Gene
- SDHA
- Location
- Chr 5233,566 (GRCh38)
- Highest magnitude
- 6.2Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon/normal
- 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 SDHA SNPs
- rs1061517A;GHereditary PGL/PCC SyndromeVery important
- rs142441643C;THereditary PGL/PCC SyndromeVery important
- rs151170408C;GHereditary PGL/PCC SyndromeVery important
- rs587782077-;GHereditary PGL/PCC SyndromeVery important
- rs746165168C;THereditary PGL/PCC SyndromeVery important
- rs781764920C;THereditary PGL/PCC SyndromeVery important
- rs786205145C;THereditary PGL/PCC SyndromeVery important
- rs876658486A;THereditary PGL/PCC SyndromeVery important
Source and license
Adapted from rs771328239 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.