rs864321686

A SNP in the COQ7 gene on chromosome 16. Its most notable genotype is A;A: Coenzyme Q10 Deficiency; severity varies

Gene
COQ7
Location
Chr 1619,075,775 (GRCh38)
Highest magnitude
5.6Very important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableBadCoenzyme Q10 Deficiency; severity variesVery important · 5.6
  2. A;TBadCarrier of a coenzyme Q10 deficiency mutationImportant · 3.0
  3. T;TGoodcommon in clinvarTypical · 0.0

On SNPedia: (A;A), (A;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Notes

From SNPedia

Notes

A;A

see coenzyme Q10 deficiency

A;T

Unaffected in absence of a second mutation; see coenzyme Q10 deficiency

Source and license

Adapted from rs864321686 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.