Complement C1q tumor necrosis factor-related protein 1 levels (C1QTNF1.6304.8.3)
CDH23 · rs10762481
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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 3,301 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.18 lower (95% confidence interval -0.12--0.24); p = 4 × 10−13.
How common The C allele had a frequency of about 38% in the people studied.
Where it sits Chromosome 10, band 10q22.1 — in an intron of CDH23.
What each result means
C/CTwo copies of the version the research linked to Complement C1q tumor necrosis factor-related protein 1 levels (C1QTNF1.6304.8.3). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Complement C1q tumor necrosis factor-related protein 1 levels (C1QTNF1.6304.8.3). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Complement C1q tumor necrosis factor-related protein 1 levels (C1QTNF1.6304.8.3). This is the starting point the study compared everyone against.
rs10762481 is a single position in the genome, in or near the CDH23 gene. Published research associates it with complement c1q tumor necrosis factor-related protein 1 levels (c1qtnf1.6304.8.3). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10762481 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs10762481 come from?
GWAS Catalog, Nature 2018, PMID:29875488. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 5122Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total5Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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