rs2315122
A SNP in the OPN1LW gene on chromosome X. Its most notable genotype is T;T: common on affy axiom data
- Gene
- OPN1LW
- Location
- Chr X154,156,369 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableGoodcommon on affy axiom data
- A;AGoodthe most common genotype as reported on DTC arrays
SNPedia records rs2315122 on the minus strand: (A;A), (T;T). 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.
- AverageT;T 99% A;A 0%
- European ancestry (Utah)T;T 100% A;A 0%
- Han Chinese (Beijing)T;T 100% A;A 0%
- Japanese (Tokyo)T;T 98% A;A 0%
- Yoruba (Nigeria)T;T 100% A;A 0%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
colorblindness https://www.23andme.com/you/community/thread/13594/
A;A
This is equivalent to rs2315122(A;A) as far as we can tell.
Source and license
Adapted from rs2315122 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.