rs786204771
A SNP in the COQ4 gene on chromosome 9. Its most notable genotype is -;-: Coenzyme Q10 Deficiency; severity varies
- Gene
- COQ4
- Location
- Chr 9128,332,271 (GRCh38)
- Highest magnitude
- 5.6Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- -;-Most notableBadCoenzyme Q10 Deficiency; severity varies
- -;CCABadCarrier of a coenzyme Q10 deficiency mutation
- CCA;CCAGoodcommon in clinvar
On SNPedia: (-;-), (-;CCA), (CCA;CCA). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other COQ4 SNPs
- rs143441644T;TCoenzyme Q10 Deficiency; severity variesVery important
- rs766317663T;TCoenzyme Q10 Deficiency; severity variesVery important
- rs774395996T;TCoenzyme Q10 Deficiency; severity variesVery important
- rs775607037T;TCoenzyme Q10 Deficiency; severity variesVery important
- rs786204770C;CCoenzyme Q10 Deficiency; severity variesVery important
Notes
From SNPedia
Notes
-;-
see coenzyme Q10 deficiency
-;CCA
Unaffected in absence of a second mutation; see coenzyme Q10 deficiency
Source and license
Adapted from rs786204771 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.