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Inguinal hernia

LINC03135 · rs115661362

Where this position leads

Condition: Inguinal Hernia

rs115661362 Condition: Inguinal Hernia Inguinal Hernia Condition rs115661362 rs115661362 LINC03135

What the study found

Who was studied 32,089 European, African, Asian, Hispanic/Latin American or mixed ancestry male cases, 196,784 European, African, Asian, Hispanic/Latin American or mixed ancestry male controls.

The effect The reported allele is C; the catalogue records no effect size ; p = 7 × 10−10.

Where it sits Chromosome 6, band 6p21.31 — inside LINC03135.

What each result means

C/C Two copies of the version the research linked to Inguinal hernia. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Inguinal hernia. That is a smaller link than two copies.
T/T No copy of the version the research linked to Inguinal hernia. This is the starting point the study compared everyone against.
Source

Questions about rs115661362

What is rs115661362?

rs115661362 is a single position in the genome, in or near the LINC03135 gene. Published research associates it with inguinal hernia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs115661362 linked to?

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

Does having rs115661362 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 rs115661362 come from?

GWAS Catalog, Human molecular genetics 2022, PMID:35022708. 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.

Inguinal hernia (rs115661362). MyGeneLog™. https://www.mygenelog.com/variants/rs115661362

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