rs80338859(C;C)

Common in clinvar

Magnitude
0.0Typical
Repute
Good
On SNPedia
rs80338859(G;G)Minus strand
Gene
DHCR7

Other genotypes of rs80338859

  1. A;CBadLikely miscall in 23andMe v4 data; otherwise: Unaffected carrier of a Smith-Lemli-Opitz syndrome mutationImportant · 3.0
  2. A;AMost notableBadMiscall for 23andMe customers; otherwise, Smith-Lemli-Opitz syndromeVery important · 9.0

All about rs80338859

Source and license

Adapted from rs80338859(G;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.