rs12467557
A SNP in the NRXN1 gene on chromosome 2. Its most notable genotype is A;A: common in complete genomics
- Gene
- NRXN1
- Location
- Chr 251,015,132 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 19%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). 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.
- AverageA;A 64%
- European ancestry (Utah)A;A 91%
- Han Chinese (Beijing)A;A 42%
- Japanese (Tokyo)A;A 42%
- Yoruba (Nigeria)A;A 81%
Related
Notes
From SNPedia
Notes
rs12467557 increases susceptibility to Substance dependence, Nicotine 1.81 times for carriers of the C allele
Source and license
Adapted from rs12467557 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.