rs1442295

A SNP in the LOC105370956 gene on chromosome 15. Its most notable genotype is T;T: common in complete genomics

Gene
LOC105370956
Location
Chr 1587,419,456 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
37%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in complete genomicsTypical · 0.036% of people

On SNPedia: (T;T). 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.

  • AverageT;T 36%
  • European ancestry (Utah)T;T 59%
  • Han Chinese (Beijing)T;T 9%
  • Japanese (Tokyo)T;T 13%
  • Yoruba (Nigeria)T;T 38%
  • African ancestry (Southwest US)T;T 39%
  • Chinese (Denver)T;T 17%
  • Gujarati IndianT;T 45%
  • Luhya (Kenya)T;T 44%
  • Mexican ancestry (Los Angeles)T;T 47%
  • Maasai (Kenya)T;T 32%
  • TuscanT;T 60%

Conditions, medicines and genes

Notes

From SNPedia

Notes

rs1442295 is a SNP in chromosome 8q24, region 1, associated both with overall risk for prostate cancer as well as disease severity, based on a meta-analysis across 10 studies.

Source and license

Adapted from rs1442295 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.