rs369711837

A SNP in the ETFDH gene on chromosome 4. Its most notable genotype is A;G: Variant of uncertain significance

Gene
ETFDH
Location
Chr 4158,699,098 (GRCh38)
Highest magnitude
2.0Worth knowing
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;GMost notableNot ratedVariant of uncertain significanceWorth knowing · 2.0
  2. G;GGoodcommon/normalTypical · 0.0

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

Other ETFDH SNPs

All ETFDH SNPs

Notes

From SNPedia

Notes

aka c.1084G>A (p.Gly362Arg) considered in ClinVar to be a variant of uncertain significance (with respect to glutaric aciduria, type 2)

A;G

see links via main rs-page

Source and license

Adapted from rs369711837 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.