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ICD10 B35.1: Tinea unguium

DSCAS · rs12958073

What the study found

Who was studied 158,152 European, African, Hispanic or Latin American and Asian ancestry cases, 1,598,198 European, African, Hispanic or Latin American and Asian ancestry controls.

The effect Each copy of the A allele shifted the measure 0.0306 lower (95% confidence interval 0.022-0.039); p = 2 × 10−12.

How common The A allele had a frequency of about 47% in the people studied.

Where it sits Chromosome 18, band 18q12.1 — in an intron of DSCAS.

What each result means

A/A Two copies of the version the research linked to ICD10 B35.1: Tinea unguium. 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 B35.1: Tinea unguium. That is a smaller link than two copies.
G/G No copy of the version the research linked to ICD10 B35.1: Tinea unguium. This is the starting point the study compared everyone against.
Source

Questions about rs12958073

What is rs12958073?

rs12958073 is a single position in the genome, in or near the DSCAS gene. Published research associates it with icd10 b35.1: tinea unguium. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs12958073 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 rs12958073 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 B35.1: Tinea unguium (rs12958073). MyGeneLog™. https://www.mygenelog.com/variants/rs12958073

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