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ICD10 B35: Dermatophytosis

DSG1-AS1 · rs61730306

What the study found

Who was studied 256,822 European, African, Hispanic or Latin American and Asian ancestry cases, 1,372,501 European, African, Hispanic or Latin American and Asian ancestry controls.

The effect Each copy of the A allele carried 0.96 times the odds of ICD10 B35: Dermatophytosis (95% confidence interval 0.9515-0.9741); p = 3 × 10−10.

How common The A allele had a frequency of about 91% in the people studied.

Where it sits Chromosome 18, band 18q12.1 — a missense change in DSG1-AS1.

What each result means

A/A Two copies of the version the research linked to ICD10 B35: Dermatophytosis. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to ICD10 B35: Dermatophytosis. That is a smaller link than two copies.
G/G No copy of the version the research linked to ICD10 B35: Dermatophytosis. This is the starting point the study compared everyone against.
Source

Questions about rs61730306

What is rs61730306?

rs61730306 is a single position in the genome, in or near the DSG1-AS1 gene. Published research associates it with icd10 b35: dermatophytosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs61730306 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 rs61730306 come from?

GWAS Catalog, Nature communications 2026, PMID:41792138. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

ICD10 B35: Dermatophytosis (rs61730306). MyGeneLog™. https://www.mygenelog.com/variants/rs61730306

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