rs1861046(G;G)

No summary available.

Magnitude
1.0Minor
Repute
Not rated
Frequency
71%Average of 11 populations
On SNPedia
rs1861046(G;G)
Gene
C1QTNF7

Frequency

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

  • European ancestry (Utah)93%
  • Tuscan92%
  • Gujarati Indian91%
  • Chinese (Denver)73%
  • Han Chinese (Beijing)69%
  • Maasai (Kenya)67%
  • Yoruba (Nigeria)64%
  • Mexican ancestry (Los Angeles)64%
  • Japanese (Tokyo)60%
  • African ancestry (Southwest US)56%
  • Luhya (Kenya)55%

Other genotypes of rs1861046

    All about rs1861046

    Notes

    From SNPedia

    Conduct disorder (CD) is one of the most prevalent childhood psychiatric conditions, and is associated with a number of serious concomitant and future problems. CD symptomatology is known to have a considerable genetic component, with heritability estimates in the range of 50%. Four SNPs reached genome-wide significance with CD symptom count, based on P < 5x10^-8 Two of these SNPs (rs16891867 and rs1861046) were in the gene C1QTNF7 (C1q and tumor necrosis factor-related protein 7). These SNPs were in high LD (r^2=0.97). The other top two SNPs meeting genome-wide significance were intergenic and located on chromosomes 11 and 13. Alleles A/G were found to be associated with CD symptom count or CD case status. downstate.edu

    Source and license

    Adapted from rs1861046(G;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.