rs3847953

A SNP in the CUX2 gene on chromosome 12. Its most notable genotype is A;G.

Gene
CUX2
Location
Chr 12111,327,660 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
41%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. A;GMost notableNot ratedNo summary available.Typical · 0.00% of people

SNPedia records rs3847953 on the minus strand: (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageA;G 0%
  • European ancestry (Utah)A;G 0%
  • Han Chinese (Beijing)A;G 0%
  • Japanese (Tokyo)A;G 0%
  • Yoruba (Nigeria)A;G 0%
  • African ancestry (Southwest US)A;G 0%
  • Chinese (Denver)A;G 0%
  • Gujarati IndianA;G 0%
  • Luhya (Kenya)A;G 0%
  • Mexican ancestry (Los Angeles)A;G 0%
  • Maasai (Kenya)A;G 0%
  • TuscanA;G 0%

Conditions, medicines and genes

Notes

From SNPedia

Notes

rs3847953 and rs933399 associated with bipolar disorder

Source and license

Adapted from rs3847953 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.