rs339445

A SNP in the DNAH5 gene on chromosome 5. Its most notable genotype is A;A: common in clinvar

Gene
DNAH5
Location
Chr 513,944,403 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
8%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in clinvarTypical · 0.0<1% of people
  2. C;CGoodcommon in complete genomicsTypical · 0.081% of people

On SNPedia: (A;A), (C;C). 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.

  • AverageA;A <1% C;C 81%
  • European ancestry (Utah)A;A <1% C;C 84%
  • Han Chinese (Beijing)A;A <1% C;C 80%
  • Japanese (Tokyo)A;A 0% C;C 81%
  • Yoruba (Nigeria)A;A 3% C;C 75%
  • African ancestry (Southwest US)A;A 2% C;C 75%
  • Chinese (Denver)A;A 0% C;C 79%
  • Gujarati IndianA;A 1% C;C 89%
  • Luhya (Kenya)A;A 2% C;C 74%
  • Mexican ancestry (Los Angeles)A;A 0% C;C 93%
  • Maasai (Kenya)A;A 1% C;C 76%
  • TuscanA;A 0% C;C 90%

Source and license

Adapted from rs339445 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.