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N-formylmethionine levels

PTRH1 · rs504434

What the study found

Who was studied 6,136 Finnish ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.22 lower; p = 4 × 10−33.

Where it sits Chromosome 9, band 9q34.11 — a missense change in PTRH1.

What each result means

A/A Two copies of the version the research linked to N-formylmethionine levels. 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 N-formylmethionine levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to N-formylmethionine levels. This is the starting point the study compared everyone against.
Source

Questions about rs504434

What is rs504434?

rs504434 is a single position in the genome, in or near the PTRH1 gene. Published research associates it with n-formylmethionine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs504434 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 rs504434 come from?

GWAS Catalog, Nature communications 2022, PMID:35347128. 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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N-formylmethionine levels (rs504434). MyGeneLog™. https://www.mygenelog.com/variants/rs504434

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