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Inguinal hernia

near Y_RNA · rs6650951

Where this position leads

Condition: Inguinal Hernia

rs6650951 Condition: Inguinal Hernia Inguinal Hernia Condition rs6650951 rs6650951 near Y_RNA

What the study found

Who was studied 13,047 European ancestry cases, 262,499 European ancestry controls; replicated in 4,450 European ancestry cases, 87,398 European ancestry controls.

The effect The reported allele is T; the catalogue records no effect size ; p = 1 × 10−13.

How common The T allele had a frequency of about 71% in the people studied.

Where it sits Chromosome 5, band 5q12.3 — between genes, 10.4 kb from Y_RNA.

What each result means

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

Questions about rs6650951

What is rs6650951?

rs6650951 is a single position in the genome, in or near the near Y_RNA 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 rs6650951 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 rs6650951 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 rs6650951 come from?

GWAS Catalog, Hernia : the journal of hernias and abdominal wall surgery 2022, PMID:34382107. 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 (rs6650951). MyGeneLog™. https://www.mygenelog.com/variants/rs6650951

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