rs12094543
A SNP in the ZMYM4 gene on chromosome 1. Its most notable genotype is A;A: >1.3x risk of type I diabetes
- Gene
- ZMYM4
- Location
- Chr 135,351,102 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 19%
Genotypes
As shown in 23andMe and AncestryDNA files.
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 4 HapMap populations.
- AverageA;A 54% A;G 32% G;G 14%
- European ancestry (Utah)A;A 97% A;G 3% G;G 0%
- Han Chinese (Beijing)A;A 16% A;G 58% G;G 27%
- Japanese (Tokyo)A;A 21% A;G 50% G;G 30%
- Yoruba (Nigeria)A;A 82% A;G 18% G;G 0%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs12094543, a SNP in the ZMYM4 gene, has been reported in a large study to be associated with type-1 diabetes. In an expanded follow-up study of >6,000 controls and 6,000 patients, the heterozygote odds ratio for this SNP was recalculated to be 1.27 (CI 1.05–1.55). Note: the risk allele is believed to be (G), but should be confirmed.
Source and license
Adapted from rs12094543 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.