rs3923890
A SNP in the ROBO3 gene on chromosome 11. Its most notable genotype is A;A: lower social interaction
- Gene
- ROBO3
- Location
- Chr 11124,870,514 (GRCh38)
- Highest magnitude
- 1.0Minor
- Tested on
- 23andMe
- Minor allele frequency
- 37%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadlower social interaction
- A;TNot ratedNo summary available.
- T;TGoodnormal social interaction
On SNPedia: (A;A), (A;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.
- AverageA;A 16% A;T 38% T;T 45%
- European ancestry (Utah)A;A 11% A;T 44% T;T 45%
- Han Chinese (Beijing)A;A 35% A;T 48% T;T 18%
- Japanese (Tokyo)A;A 27% A;T 48% T;T 25%
- Yoruba (Nigeria)A;A <1% A;T 19% T;T 80%
- African ancestry (Southwest US)A;A 9% A;T 25% T;T 66%
- Chinese (Denver)A;A 35% A;T 46% T;T 19%
- Gujarati IndianA;A 17% A;T 47% T;T 37%
- Luhya (Kenya)A;A <1% A;T 29% T;T 70%
- Mexican ancestry (Los Angeles)A;A 28% A;T 48% T;T 24%
- Maasai (Kenya)A;A 3% A;T 28% T;T 69%
- TuscanA;A 13% A;T 40% T;T 47%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs3923890 has been reported to be a SNP potentially associated with increased risk for autism
A;A
Increased risk of autism. Lower social interaction on ADI-R_A test.ncbi.nlm.nih.gov
T;T
Normal autism risk.ncbi.nlm.nih.gov
Source and license
Adapted from rs3923890 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.