rs111033824
A SNP in the IL11RA gene on chromosome 9. Its most notable genotype is C;C: Galactosemia (predicted); see discussion
- Gene
- IL11RA
- Location
- Chr 934,650,447 (GRCh38)
- Highest magnitude
- 8.0Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableBadGalactosemia (predicted); see discussion
- C;TBadCarrier of a GALT gene mutation
- T;TGoodcommon in clinvar
On SNPedia: (C;C), (C;T), (T;T). 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
c.1138T>C (p.Ter380Arg) 23andMe name: i5012722
C;C
See discussion at GALT gene; condition is treated by dietary modifications.
C;T
Unaffected in absence of a second GALT gene mutation; see discussion at the GALT gene page.
Source and license
Adapted from rs111033824 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.