rs9282859
A SNP in the STK11 gene on chromosome 19. Its most notable genotype is C;G: STK11 gene mutation associated with Peutz-Jeghers syndrome
- Gene
- STK11
- Location
- Chr 191,221,294 (GRCh38)
- Highest magnitude
- 5.8Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon/normal
- C;GMost notableBadSTK11 gene mutation associated with Peutz-Jeghers syndrome
On SNPedia: (C;C), (C;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other STK11 SNPs
- rs121913315A;GSTK11 gene mutation associated with Peutz-Jeghers syndromeVery important
- rs121913321-;CSTK11 gene mutation associated with Peutz-Jeghers syndromeVery important
- rs121913322C;TSTK11 gene mutation associated with Peutz-Jeghers syndromeVery important
- rs121913324C;TSTK11 gene mutation associated with Peutz-Jeghers syndromeVery important
- rs137853075A;CLikely miscall in Ancestry v2c data; otherwise, STK11 gene mutation associated with Peutz-Jeghers syndromeVery important
- rs137853076A;TSTK11 gene mutation associated with Peutz-Jeghers syndromeVery important
- rs137853077C;TSTK11 gene mutation associated with Peutz-Jeghers syndromeVery important
- rs137853078A;GSTK11 gene mutation associated with Peutz-Jeghers syndromeVery important
Notes
From SNPedia
Notes
C;G
Very rare condition; false positives are possible.
Source and license
Adapted from rs9282859 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.