rs7014851

A SNP in the HR gene on chromosome 8. Its most notable genotype is C;C.

Gene
HR
Location
Chr 822,119,197 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
8%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableNot ratedNo summary available.Typical · 0.03% of people
  2. C;TGoodVery likely to be a benign alleleTypical · 0.015% of people
  3. T;TGoodcommonTypical · 0.081% of people

On SNPedia: (C;C), (C;T), (T;T). 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;C 3% C;T 15% T;T 81%
  • European ancestry (Utah)C;C <1% C;T <1% T;T 98%
  • Han Chinese (Beijing)C;C 0% C;T <1% T;T 99%
  • Japanese (Tokyo)C;C 0% C;T 0% T;T 100%
  • Yoruba (Nigeria)C;C 11% C;T 48% T;T 42%
  • African ancestry (Southwest US)C;C 9% C;T 35% T;T 56%
  • Gujarati IndianC;C 0% C;T 1% T;T 99%
  • Luhya (Kenya)C;C 6% C;T 32% T;T 62%
  • Mexican ancestry (Los Angeles)C;C 0% C;T 3% T;T 97%
  • Maasai (Kenya)C;C 5% C;T 31% T;T 64%
  • TuscanC;C 0% C;T 3% T;T 97%

Source and license

Adapted from rs7014851 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.