rs11911134
GRM7rs11911134 is a single-nucleotide polymorphism (SNP) in the GRM7 gene. Genespiral reads it in the Aging & Longevity analysis to describe Age-related Hearing Loss.
- Gene
- GRM7
- Alleles
- C / T
- Genotypes
- TT, TC, CC
- Traits
- 1 trait across 1 analysis
An rsID such as rs11911134 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 TT, TC, CC. The order of the two letters carries no meaning, so TC 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.
Age-related Hearing Loss
Sensory Aging · Part of the Aging & Longevity analysis
Involved in auditory neuron signaling.
| Genotype | Association |
|---|---|
| TT | Typical hearing aging pattern |
| TC | Modest variation in pattern |
| CC | Slight protective association |
- Summary
- One of multiple genes affecting age-related hearing.
- Scientific insights
- Environmental factors like noise exposure often more significant.
- Lifestyle tips
- Protecting ears from loud noise important for all genotypes.
Check your genotype at rs11911134
Load your raw DNA file and Genespiral looks up rs11911134 along with every other marker in the Aging & Longevity 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 Age-related Hearing Loss 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 rs11911134 - NCBI
- rs11911134 variant page - Ensembl
- rs11911134 summary - SNPedia
- Clinical significance records for rs11911134 - ClinVar
- GRM7 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.