rs7927894
C11orf30rs7927894 is a single-nucleotide polymorphism (SNP) in the C11orf30 gene. Genespiral reads it in the Health & Wellness analysis to describe Eczema Risk.
- Gene
- C11orf30
- Alleles
- C / T
- Genotypes
- CC, CT, TT
- Traits
- 1 trait across 1 analysis
An rsID such as rs7927894 is the reference number dbSNP assigns to one position in the genome where people commonly differ by a single letter. Raw data exports from 23andMe and AncestryDNA list your two alleles at that position as a genotype - for this marker one of CC, CT, TT. The order of the two letters carries no meaning, so CT and its reverse are the same genotype.
Alleles on this page are written on the forward (plus) strand, matching how consumer raw files report them. Other references sometimes describe the same variant on the opposite strand, which swaps A↔T and C↔G - see why the same variant can look different. The associations below are educational summaries of published research; they are not diagnoses, and the effect of any single SNP is usually modest.
Eczema Risk
Skin and Hair Conditions · Part of the Health & Wellness analysis
Plays a role in immune function, influencing eczema susceptibility.
| Genotype | Association |
|---|---|
| CC | Increased Risk |
| CT | Moderate Risk |
| TT | Lower Risk |
- Summary
- C11orf30 gene variations affect an individual’s likelihood of developing eczema.
- Scientific insights
- 'CC' genotype individuals are more prone to eczema and may experience more severe symptoms.
- Lifestyle tips
- Using hypoallergenic products can help reduce eczema flare-ups.
Check your genotype at rs7927894
Load your raw DNA file and Genespiral looks up rs7927894 along with every other marker in the Health & Wellness analysis. The file is parsed in your browser and never uploaded, so your genotype stays on your device.
- 1. Download your raw data from 23andMe or AncestryDNA.
- 2. Open the analysis below and choose the file.
- 3. Find Eczema Risk in your results.
Related
References
Primary databases for this variant. Use them to check allele orientation, population frequencies, and the underlying studies.
- dbSNP entry for rs7927894 - NCBI
- rs7927894 variant page - Ensembl
- rs7927894 summary - SNPedia
- Clinical significance records for rs7927894 - ClinVar
- C11orf30 gene - NCBI Gene
Genespiral is an educational tool, not a medical service. Genetic associations describe tendencies observed across populations, not certainties for you. Read the full disclaimer.