rs6161(C;T)

Carrier of a likely primary adrenal insufficiency mutation

Magnitude
3.0Important
Repute
Bad
Frequency
1%Average of 7 populations
On SNPedia
rs6161(A;G)Minus strand
Gene
CYP11A1

Frequency

Share of people with C;T in each HapMap population.

  • Mexican ancestry (Los Angeles)4%
  • Tuscan1%
  • European ancestry (Utah)<1%
  • Japanese (Tokyo)<1%
  • Luhya (Kenya)<1%
  • Han Chinese (Beijing)<1%
  • Yoruba (Nigeria)<1%

Other genotypes of rs6161

  1. C;CGoodcommon in clinvarTypical · 0.099% of people

All about rs6161

Notes

From SNPedia

Unaffected in absence of a second CYP11A1 gene mutation; see text on main rs-page.

Source and license

Adapted from rs6161(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.