rs1552311

A SNP in the LOC107984755 gene on chromosome 15. Its most notable genotype is C;C: common in complete genomics

Gene
LOC107984755
Location
Chr 1548,288,516 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
<1%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in complete genomicsTypical · 0.098% of people
  2. T;TGoodcommon in clinvarTypical · 0.00% of people

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

Frequency

Share of each genotype in 8 HapMap populations.

  • AverageC;C 98% T;T 0%
  • European ancestry (Utah)C;C 99% T;T 0%
  • Han Chinese (Beijing)C;C 99% T;T 0%
  • Japanese (Tokyo)C;C 98% T;T 0%
  • Yoruba (Nigeria)C;C 97% T;T 0%
  • Chinese (Denver)C;C 99% T;T 0%
  • Luhya (Kenya)C;C 96% T;T 0%
  • Mexican ancestry (Los Angeles)C;C 97% T;T 0%
  • Maasai (Kenya)C;C 97% T;T 0%

Source and license

Adapted from rs1552311 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.