rs189798
A SNP on chromosome 8. Its most notable genotype is A;A: decreased high myopia risk
- Gene
- None listed
- Location
- Chr 89,133,067 (GRCh38)
- Highest magnitude
- 2.1Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 38%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GNot ratednormal high myopia risk
- A;GGooddecreased high myopia risk
- A;AMost notableGooddecreased high myopia risk
SNPedia records rs189798 on the minus strand: (C;C), (C;T), (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.
- AverageG;G 40% A;G 40% A;A 21%
- European ancestry (Utah)G;G 59% A;G 34% A;A 7%
- Han Chinese (Beijing)G;G 12% A;G 39% A;A 48%
- Japanese (Tokyo)G;G 15% A;G 47% A;A 38%
- Yoruba (Nigeria)G;G 61% A;G 35% A;A 4%
- African ancestry (Southwest US)G;G 60% A;G 35% A;A 5%
- Chinese (Denver)G;G 17% A;G 38% A;A 46%
- Gujarati IndianG;G 30% A;G 52% A;A 19%
- Luhya (Kenya)G;G 53% A;G 39% A;A 8%
- Mexican ancestry (Los Angeles)G;G 26% A;G 40% A;A 35%
- Maasai (Kenya)G;G 63% A;G 33% A;A 4%
- TuscanG;G 40% A;G 47% A;A 13%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
G;G
Normal (higher) risk of high myopia (in French people).(table)
A;G
Less risk of high myopia (in French people). 34.2% of French people without high myopia have T here, but only 21.1% of controls do.(table)
A;A
Less risk of high myopia (in French people). 34.2% of French people without high myopia have T here, but only 21.1% of controls do.(table)
References
Source and license
Adapted from rs189798 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.