rs786201012

A SNP in the KIF14 gene on chromosome 1. Its most notable genotype is -;GA: Carrier of a Meckel syndrome mutation (type 12)

Gene
KIF14
Location
Chr 1200,603,951 (GRCh38)
Highest magnitude
3.0Important
Tested on
AncestryDNA

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. -;GAMost notableBadCarrier of a Meckel syndrome mutation (type 12)Important · 3.0
  2. GA;GAGoodcommon in clinvarTypical · 0.0

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

Notes

From SNPedia

Notes

-;GA

Unaffected in absence of a second KIF14 gene mutation

Source and license

Adapted from rs786201012 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.