rs397514561

A SNP in the DNAAF5 gene on chromosome 7. Its most notable genotype is C;T: Carrier for a primary ciliary dyskinesia-18 mutation

Gene
DNAAF5
Location
Chr 7780,097 (GRCh38)
Highest magnitude
3.0Important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;TMost notableBadCarrier for a primary ciliary dyskinesia-18 mutationImportant · 3.0
  2. T;TGoodcommon in clinvarTypical · 0.0

On SNPedia: (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Notes

From SNPedia

Notes

see OMIM 614864.0001

C;T

Unaffected in absence of a second DNAAF5 gene mutation

Source and license

Adapted from rs397514561 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.