rs2675703
A SNP in the OPN4 gene on chromosome 10. Its most notable genotype is C;C: common on affy axiom data
- Gene
- OPN4
- Location
- Chr 1086,654,812 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 9%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableGoodcommon on affy axiom data
- T;TNot rated5.6x more likely to have seasonal affective disorder (SAD)
On SNPedia: (C;C), (T;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.
- AverageC;C 83% T;T 1%
- European ancestry (Utah)C;C 73% T;T 3%
- Han Chinese (Beijing)C;C 96% T;T <1%
- Japanese (Tokyo)C;C 87% T;T 0%
- Yoruba (Nigeria)C;C 96% T;T 0%
- African ancestry (Southwest US)C;C 91% T;T 2%
- Chinese (Denver)C;C 93% T;T 0%
- Gujarati IndianC;C 80% T;T 1%
- Luhya (Kenya)C;C 92% T;T 0%
- Mexican ancestry (Los Angeles)C;C 74% T;T 5%
- Maasai (Kenya)C;C 76% T;T 1%
- TuscanC;C 61% T;T 3%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
T;T
This SNP in the melanopsin OPN4 gene is associated with seasonal affective disorder, according to one study with 130 affected participants. PMID 18804284
References
Source and license
Adapted from rs2675703 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.