rs797044465

A SNP in the KIF7 gene on chromosome 15. Its most notable genotype is -;C: Possible miscall in Ancestry v2c data; otherwise, carrier of a Joubert syndrome mutation

Gene
KIF7
Location
Chr 1589,652,714 (GRCh38)
Highest magnitude
3.0Important
Tested on
AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. -;CMost notableBadPossible miscall in Ancestry v2c data; otherwise, carrier of a Joubert syndrome mutationImportant · 3.0
  2. C;CGoodcommon in clinvarTypical · 0.0

SNPedia records rs797044465 on the minus strand: (-;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Other KIF7 SNPs

All KIF7 SNPs

Notes

From SNPedia

Notes

aka c.217delG (p.Ala73Profs)

-;C

Unaffected in absence of a second mutation in the KIF7 gene; see links via main rs-page.

Source and license

Adapted from rs797044465 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.