rs2309689(A;G)

Carrier of a VLCAD deficiency mutation

Magnitude
3.0Important
Repute
Bad
Frequency
<1%Average of 7 populations
On SNPedia
rs2309689(A;G)
Gene
ACADVL

Frequency

Share of people with A;G in each HapMap population.

  • Mexican ancestry (Los Angeles)2%
  • Japanese (Tokyo)<1%
  • Luhya (Kenya)<1%
  • Han Chinese (Beijing)<1%
  • Maasai (Kenya)<1%
  • European ancestry (Utah)0%
  • Yoruba (Nigeria)0%

Other genotypes of rs2309689

  1. G;GGoodcommon in clinvarTypical · 0.099% of people

All about rs2309689

Notes

From SNPedia

Unaffected in absence of a second ACADVL gene mutation

Source and license

Adapted from rs2309689(A;G) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.