rs13078881(C;C)

Biotinidase deficiency; note ability to treat & variable penetrance

Magnitude
6.7Very important
Repute
Bad
Frequency
0%Average of 4 populations
On SNPedia
rs13078881(C;C)
Gene
BTD

Frequency

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

  • European ancestry (Utah)0%
  • Han Chinese (Beijing)0%
  • Japanese (Tokyo)0%
  • Yoruba (Nigeria)0%

Other genotypes of rs13078881

  1. C;GBadCarrier of a biotinidase deficiency mutationImportant · 3.01% of people
  2. G;GGoodcommon in clinvarTypical · 0.099% of people

All about rs13078881

Notes

From SNPedia

see rs13078881

Source and license

Adapted from rs13078881(C;C) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.