rs10902758

A SNP in the LOC101928521 gene on chromosome 4. Its most notable genotype is A;A: common in complete genomics

Gene
LOC101928521
Location
Chr 4654,854 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
<1%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in complete genomicsTypical · 0.098% of people
  2. G;GGoodcommon in clinvarTypical · 0.00% of people

On SNPedia: (A;A), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 2 HapMap populations.

  • AverageA;A 98% G;G 0%
  • Luhya (Kenya)A;A 99% G;G 0%
  • Maasai (Kenya)A;A 97% G;G 0%

Source and license

Adapted from rs10902758 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.