rs2032652
A SNP in the LOC105377224 gene on chromosome Y. Its most notable genotype is T;T.
- Gene
- LOC105377224
- Location
- Chr Y19,755,427 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 28%
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 4 HapMap populations.
- AverageT;T 59%
- European ancestry (Utah)T;T 100%
- Han Chinese (Beijing)T;T 91%
- Japanese (Tokyo)T;T 46%
- Yoruba (Nigeria)T;T 0%
Related
Genosets
Genosets combine several genotypes. Twofold checks them in your report.
Notes
From SNPedia
Notes
In silico and in vitro comparative analysis to select, validate and test SNPs for human identification. MEGF10 association with schizophrenia. FBXL21 association with schizophrenia in Irish family and case-control samples. Association of Y chromosome haplogroup I with HIV progression, and HAART outcome.
Source and license
Adapted from rs2032652 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.