rs761100
A SNP in the KIAA0319 gene on chromosome 6. Its most notable genotype is C;C: higher risk for dyslexia
- Gene
- KIAA0319
- Location
- Chr 624,632,414 (GRCh38)
- Highest magnitude
- 1.0Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 32%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs761100 on the minus strand: (G;G), (G;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.
- AverageC;C 53% A;C 38% A;A 9%
- European ancestry (Utah)C;C 26% A;C 57% A;A 17%
- Han Chinese (Beijing)C;C 75% A;C 24% A;A <1%
- Japanese (Tokyo)C;C 83% A;C 16% A;A <1%
- Yoruba (Nigeria)C;C 50% A;C 39% A;A 11%
- African ancestry (Southwest US)C;C 51% A;C 44% A;A 5%
- Chinese (Denver)C;C 81% A;C 18% A;A <1%
- Gujarati IndianC;C 35% A;C 53% A;A 13%
- Luhya (Kenya)C;C 53% A;C 42% A;A 6%
- Mexican ancestry (Los Angeles)C;C 52% A;C 43% A;A 5%
- Maasai (Kenya)C;C 47% A;C 40% A;A 13%
- TuscanC;C 28% A;C 48% A;A 24%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
The more common allele of rs761100 has been linked to increased risk for developmental dyslexia in a study of ~300 British families. While odds ratios were not reported, the significance was reported as p=0.02. Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment. Developmental Dyslexia
Source and license
Adapted from rs761100 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.