rs1805165

A SNP in the LOC101928371 gene on chromosome 2. Its most notable genotype is C;C: common in clinvar

Gene
LOC101928371
Location
Chr 288,575,373 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
29%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.09% of people

SNPedia records rs1805165 on the minus strand: (G;G). 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 9%
  • European ancestry (Utah)C;C 8%
  • Han Chinese (Beijing)C;C 21%
  • Japanese (Tokyo)C;C 18%
  • Yoruba (Nigeria)C;C 0%
  • African ancestry (Southwest US)C;C 0%
  • Chinese (Denver)C;C 25%
  • Gujarati IndianC;C 17%
  • Luhya (Kenya)C;C 0%
  • Mexican ancestry (Los Angeles)C;C 7%
  • Maasai (Kenya)C;C <1%
  • TuscanC;C 7%

Conditions, medicines and genes

Notes

From SNPedia

Notes

Progressive Supranuclear Palsy

Source and license

Adapted from rs1805165 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.