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ICD10 K44: Diaphragmatic hernia

near TMEM59L · rs78484848

What the study found

Who was studied 275,546 individuals; replicated in 91,850 individuals.

The effect The reported allele is T; the catalogue records no effect size ; p = 2 × 10−11.

Where it sits Chromosome 19, band 19p13.11 — between genes, 0.6 kb from TMEM59L.

What each result means

C/C No copy of the version the research linked to ICD10 K44: Diaphragmatic hernia. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to ICD10 K44: Diaphragmatic hernia. That is a smaller link than two copies.
T/T Two copies of the version the research linked to ICD10 K44: Diaphragmatic hernia. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs78484848

What is rs78484848?

rs78484848 is a single position in the genome, in or near the near TMEM59L gene. Published research associates it with icd10 k44: diaphragmatic hernia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs78484848 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 rs78484848 come from?

GWAS Catalog, Surgical endoscopy 2022, PMID:36076102. 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 K44: Diaphragmatic hernia (rs78484848). MyGeneLog™. https://www.mygenelog.com/variants/rs78484848

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