rs5934953
A SNP in the MID1 gene on chromosome X. Its most notable genotype is T;T: common on affy axiom data
- Gene
- MID1
- Location
- Chr X11,030,572 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 1%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 6 HapMap populations.
- AverageT;T 98%
- European ancestry (Utah)T;T 93%
- Han Chinese (Beijing)T;T 100%
- Japanese (Tokyo)T;T 100%
- Yoruba (Nigeria)T;T 100%
- Gujarati IndianT;T 98%
- TuscanT;T 96%
Notes
From SNPedia
Notes
non sig. gwas, top hit for paired associates learning (PAL) total errors at 6 patterns in the CANTAB (Cambridge Neuropsychological Test Automated Battery)
Source and license
Adapted from rs5934953 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.