rs2309689

A SNP in the ACADVL gene on chromosome 17. Its most notable genotype is A;G: Carrier of a VLCAD deficiency mutation

Gene
ACADVL
Location
Chr 177,223,865 (GRCh38)
Highest magnitude
3.0Important
Tested on
23andMe, AncestryDNA, FamilyTreeDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;GMost notableBadCarrier of a VLCAD deficiency mutationImportant · 3.0<1% of people
  2. G;GGoodcommon in clinvarTypical · 0.099% of people

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

Frequency

Share of each genotype in 7 HapMap populations.

  • AverageA;G <1% G;G 99%
  • European ancestry (Utah)A;G 0% G;G 100%
  • Han Chinese (Beijing)A;G <1% G;G 99%
  • Japanese (Tokyo)A;G <1% G;G 99%
  • Yoruba (Nigeria)A;G 0% G;G 100%
  • Luhya (Kenya)A;G <1% G;G 99%
  • Mexican ancestry (Los Angeles)A;G 2% G;G 98%
  • Maasai (Kenya)A;G <1% G;G 99%

Other ACADVL SNPs

All ACADVL SNPs

Notes

From SNPedia

Notes

A;G

Unaffected in absence of a second ACADVL gene mutation

Source and license

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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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