rs2024513
A SNP in the NRXN1 gene on chromosome 2. Its most notable genotype is A;A: 1.7x higher risk for schizophrenia (among Han Chinese)
- Gene
- NRXN1
- Location
- Chr 250,924,881 (GRCh38)
- Highest magnitude
- 1.7Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 28%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBad1.7x higher risk for schizophrenia (among Han Chinese)
- A;GBad1.3x higher risk for schizophrenia (among Han Chinese)
- G;GNot ratedNo summary available.
On SNPedia: (A;A), (A;G), (G;G). 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 63% A;G 30% G;G 6%
- European ancestry (Utah)A;A 31% A;G 45% G;G 24%
- Han Chinese (Beijing)A;A 64% A;G 33% G;G 3%
- Japanese (Tokyo)A;A 67% A;G 29% G;G 5%
- Yoruba (Nigeria)A;A 90% A;G 10% G;G <1%
- African ancestry (Southwest US)A;A 68% A;G 32% G;G 0%
- Chinese (Denver)A;A 68% A;G 28% G;G 4%
- Gujarati IndianA;A 59% A;G 37% G;G 4%
- Luhya (Kenya)A;A 89% A;G 11% G;G 0%
- Mexican ancestry (Los Angeles)A;A 50% A;G 36% G;G 14%
- Maasai (Kenya)A;A 72% A;G 27% G;G 1%
- TuscanA;A 39% A;G 46% G;G 15%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs2024513 is a SNP in the neurexin-1 NRXN1 gene on chromosome 2p16.3. Based on a case-control study of 700+ Han Chinese patients with schizophrenia, rs2024513(A) was associated with higher risk, at an odds ratio of 1.3 (CI: 1.07 - 1.56, p=0.006).
Source and license
Adapted from rs2024513 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.