rs10510089

A SNP in the LOC105378522 gene on chromosome 10. Its most notable genotype is C;T.

Gene
LOC105378522
Location
Chr 10121,148,705 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe
Minor allele frequency
10%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;TMost notableNot ratedNo summary available.Typical · 0.025% of people
  2. T;TGoodcommon in complete genomicsTypical · 0.071% of people

On SNPedia: (C;T), (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.

  • AverageC;T 25% T;T 71%
  • European ancestry (Utah)C;T 0% T;T 100%
  • Han Chinese (Beijing)C;T 27% T;T 64%
  • Japanese (Tokyo)C;T 30% T;T 66%
  • Yoruba (Nigeria)C;T 43% T;T 54%

Other LOC105378522 SNPs

All LOC105378522 SNPs

Source and license

Adapted from rs10510089 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.