rs79967166
A SNP in the DNAH5 gene on chromosome 5. Its most notable genotype is C;G: Unaffected carrier of a ciliary dyskinesia mutation
- Gene
- DNAH5
- Location
- Chr 513,754,203 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;GMost notableBadUnaffected carrier of a ciliary dyskinesia mutation
- C;CGoodcommon in clinvar
SNPedia records rs79967166 on the minus strand: (C;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Notes
From SNPedia
Notes
aka c.10555G>C (p.Gly3519Arg) FTDNA & MyHeritage name: VG05S26940
C;G
see links via main rs-page
Source and license
Adapted from rs79967166 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.