rs1063739

A SNP in the LOC101928953 gene on chromosome 8. Its most notable genotype is C;C: common in clinvar

Gene
LOC101928953
Location
Chr 8144,504,344 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
42%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.042% of people

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

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageC;C 42%
  • European ancestry (Utah)C;C 32%
  • Han Chinese (Beijing)C;C 32%
  • Japanese (Tokyo)C;C 35%
  • Yoruba (Nigeria)C;C 67%
  • African ancestry (Southwest US)C;C 70%
  • Chinese (Denver)C;C 27%
  • Gujarati IndianC;C 13%
  • Luhya (Kenya)C;C 66%
  • Mexican ancestry (Los Angeles)C;C 24%
  • Maasai (Kenya)C;C 71%
  • TuscanC;C 28%

Notes

From SNPedia

Notes

[SNP pentaplex--the allele frequency database of central Poland population]. [The central Poland population database of 500 SNP alleles]. [The usefulness of SNP markers for analyses of highly degraded biological materials].

Source and license

Adapted from rs1063739 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.