rs1917445

A SNP on chromosome 11. Its most notable genotype is C;T: common in complete genomics

Gene
None listed
Location
Chr 11103,718,366 (GRCh38)
Highest magnitude
0.0Typical
Tested on
AncestryDNA
Minor allele frequency
47%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;TMost notableGoodcommon in complete genomicsTypical · 0.043% of people

SNPedia records rs1917445 on the minus strand: (A;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 10 HapMap populations.

  • AverageC;T 43%
  • European ancestry (Utah)C;T 50%
  • Han Chinese (Beijing)C;T 48%
  • Japanese (Tokyo)C;T 40%
  • African ancestry (Southwest US)C;T 28%
  • Chinese (Denver)C;T 56%
  • Gujarati IndianC;T 42%
  • Luhya (Kenya)C;T 20%
  • Mexican ancestry (Los Angeles)C;T 47%
  • Maasai (Kenya)C;T 37%
  • TuscanC;T 58%

Source and license

Adapted from rs1917445 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.