rs8192466(A;A)

Uncertain

Magnitude
4.0Very important
Repute
Not rated
Frequency
0%Average of 5 populations
On SNPedia
rs8192466(T;T)Minus strand
Gene
BDNF

Frequency

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

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

Other genotypes of rs8192466

  1. G;GGoodcommonTypical · 0.0100% of people
  2. A;GNot rateduncertain, probably harmlessWorth knowing · 2.5<1% of people

All about rs8192466

Notes

From SNPedia

According to ClinVar this is Pathogenic for Congenital central hypoventilation, and according to HapMap it's quite rare. However The heterozygous form seems to be occurring in quite a few Promethease reports from healthy people. We now suspect this is being incorrectly genotyped by 23andMe, but it remains uncertain. If you've found it in your promethease report info@snpedia.com would like to hear from you.

Source and license

Adapted from rs8192466(T;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.