rs148833559
A SNP in the STC2 gene on chromosome 5. Its most notable genotype is A;C: Height-related; on average, 2cm taller than non-carriers
- Gene
- STC2
- Location
- Chr 5173,328,063 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;CMost notableNot ratedHeight-related; on average, 2cm taller than non-carriers
- C;CGoodcommon/normal
On SNPedia: (A;C), (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
- Height related SNP; carriers of the (rare) minor allele for this STC2 gene missense variant are approximately 2.1cm taller than non-carriers.
A;C
see citations at rs148833559
Source and license
Adapted from rs148833559 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.