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Inguinal hernia

ADAMTS16-AS1 · rs1834922

Where this position leads

Condition: Inguinal Hernia

rs1834922 Condition: Inguinal Hernia Inguinal Hernia Condition rs1834922 rs1834922 ADAMTS16-AS1

What the study found

Who was studied 33,379 European ancestry cases, 436,717 European ancestry controls.

The effect Each copy of the A allele shifted the measure 0.0501 lower (95% confidence interval 0.033-0.067); p = 1 × 10−8.

Where it sits Chromosome 5, band 5p15.32 — in an intron of ADAMTS16-AS1.

What each result means

A/A 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.
A/G One copy of the version the research linked to Inguinal hernia. That is a smaller link than two copies.
G/G No copy of the version the research linked to Inguinal hernia. This is the starting point the study compared everyone against.
Source

Questions about rs1834922

What is rs1834922?

rs1834922 is a single position in the genome, in or near the ADAMTS16-AS1 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 rs1834922 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 rs1834922 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 rs1834922 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 (rs1834922). MyGeneLog™. https://www.mygenelog.com/variants/rs1834922

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