rs11555217(C;T)

Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs11555217(A;G)Minus strand
Gene
DHCR7

Other genotypes of rs11555217

  1. C;CGoodcommon in clinvarTypical · 0.0

All about rs11555217

Notes

From SNPedia

see Smith-Lemli-Opitz syndrome

Source and license

Adapted from rs11555217(A;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.