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Viral Enteritis (PheCode 8.6)

MAPK14 · rs150335499

What the study found

Who was studied 466 African American or Afro-Caribbean cases, 118,792 African American or Afro-Caribbean controls, 1,327 European ancestry cases, 442,946 European ancestry controls.

The effect Each copy of the G allele shifted the measure 1.68 lower (95% confidence interval 1.61-1.75); p = 6 × 10−13.

How common The G allele had a frequency of about 100% in the people studied.

Where it sits Chromosome 6, band 6p21.31 — in an intron of MAPK14.

What each result means

A/A No copy of the version the research linked to Viral Enteritis (PheCode 8.6). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Viral Enteritis (PheCode 8.6). That is a smaller link than two copies.
G/G Two copies of the version the research linked to Viral Enteritis (PheCode 8.6). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs150335499

What is rs150335499?

rs150335499 is a single position in the genome, in or near the MAPK14 gene. Published research associates it with viral enteritis (phecode 8.6). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs150335499 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 rs150335499 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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Viral Enteritis (PheCode 8.6) (rs150335499). MyGeneLog™. https://www.mygenelog.com/variants/rs150335499

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