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ICD10 B35: Dermatophytosis

RTEL1 · rs2236506

Where this position leads

Condition: Dermatophytosis

rs2236506 Condition: Dermatophytosis Dermatophytosis Condition rs2236506 rs2236506 RTEL1

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 0.97 times the odds of ICD10 B35: Dermatophytosis (95% confidence interval 0.959-0.9742); p = 9 × 10−15.

How common The A allele had a frequency of about 78% in the people studied.

Where it sits Chromosome 20, band 20q13.33 — a missense change in RTEL1.

What ClinVar records

Classification Benign/Likely benign for Dyskeratosis congenita, Dyskeratosis congenita, autosomal recessive 5, Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 14 submitters), last evaluated 2026-02-04. ClinVar record 403400 NM_001283009.2(RTEL1):c.2274G>A (p.Ala758=)

What this is ClinVar's aggregate record for this position (as of its 2026-10-12 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

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 rs2236506

What is rs2236506?

rs2236506 is a single position in the genome, in or near the RTEL1 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.

What conditions is rs2236506 linked to?

On MyGeneLog this position is linked to Dermatophytosis. The research behind each link, and its sources, are set out on that condition page.

Does having rs2236506 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 rs2236506 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

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ICD10 B35: Dermatophytosis (rs2236506). MyGeneLog™. https://www.mygenelog.com/variants/rs2236506

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