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Hepatitis

CCDC148 · rs72936092

Where this position leads

What the study found

Who was studied 26 Vis (founder/genetic isolate) cases, 30 Korculan (founder/genetic isolate) cases, 20 Split cases, 934 Vis (founder/genetic isolate) controls, 2,668 Korculan (founder/genetic isolate) controls, 946 Split controls.

The effect Each copy of the A allele carried 1.16 times the odds of Hepatitis (95% confidence interval 1.11-1.2); p = 9 × 10⁻¹¹.

How common The A allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 2, band 2q24.1 — in an intron of CCDC148.

What each result means

A/A Two copies of the version the research linked to Hepatitis. 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 Hepatitis. That is a smaller link than two copies.

G/G No copy of the version the research linked to Hepatitis. This is the starting point the study compared everyone against.

Source

Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk

Gelemanović A, Ćatipović Ardalić T, Pribisalić A, Hayward C, Kolčić I, Polašek O

International journal of molecular sciences · 2023 · PMID 37108169 · open access

Questions about rs72936092

What is rs72936092?

rs72936092 is a single position in the genome, in or near the CCDC148 gene. Published research associates it with hepatitis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs72936092 linked to?

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

Does having rs72936092 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 rs72936092 come from?

GWAS Catalog, International journal of molecular sciences 2023, PMID:37108169. 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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Hepatitis (rs72936092). MyGeneLog™. https://www.mygenelog.com/variants/rs72936092

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