rs113994168
A SNP in the ACADVL gene on chromosome 17. Its most notable genotype is C;T: Carrier of a ACADVL gene mutation
- Gene
- ACADVL
- Location
- Chr 177,222,203 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- C;TMost notableBadCarrier of a ACADVL gene mutation
On SNPedia: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other ACADVL SNPs
- rs113994167C;CVLCAD deficiency (predicted)Very important
- rs2309689A;GCarrier of a VLCAD deficiency mutationImportant
- rs118204015A;CCarrier of a VLCAD deficiency mutationImportant
- rs118204017C;TCarrier of a VLCAD deficiency mutationImportant
- rs140629318A;GCarrier of a (likely) VLCAD mutationImportant
- rs140989450G;TCarrier of a VLCAD deficiency mutationImportant
- rs200788251A;GCarrier of a VLCAD deficiency mutationImportant
- rs387906249-;GCarrier of a VLCAD deficiency mutationImportant
Notes
From SNPedia
Notes
aka c.779C>T (p.Thr260Met or T260M)
C;T
Unaffected in absence of a second ACADVL gene mutation
Source and license
Adapted from rs113994168 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.