rs150414818

A SNP in the ALDH16A1 gene on chromosome 19. Its most notable genotype is G;G: increased risk of gout

Gene
ALDH16A1
Location
Chr 1949,465,749 (GRCh38)
Highest magnitude
3.5Important
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CNot ratedNo summary available.Typical · 0.0
  2. G;GMost notableBadincreased risk of goutImportant · 3.5

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

Notes

From SNPedia

Notes

a low-frequency missense variant rs150414818 (c.1580C>G) in ALDH16A1 associated with gout (OR = 3.12, P = 1.5 × 10?16, at-risk allele frequency = 0.019) and serum uric acid levels (effect = 0.36 s.d., P = 4.5 × 10?21) nature genetics

Source and license

Adapted from rs150414818 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.