rs4792887
A SNP in the CRHR1-IT1-CRHR1 gene on chromosome 17. Its most notable genotype is C;C: common in complete genomics
- Gene
- CRHR1-IT1-CRHR1
- Location
- Chr 1745,799,654 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 13%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageC;C 83%
- European ancestry (Utah)C;C 88%
- Han Chinese (Beijing)C;C 100%
- Japanese (Tokyo)C;C 100%
- Yoruba (Nigeria)C;C 43%
Related
Notes
From SNPedia
Notes
family trios with suicide attempter offspring (n = 542) rs4792887 linked to suicide attempters exposed to low levels of stress (P = 0.002), among whom most males were depressed (P = 0.001).
Source and license
Adapted from rs4792887 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.