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Phenylalanylphenylalanine levels

ABCC1 · rs2062541

What the study found

Who was studied 6,136 Finnish ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.23 higher; p = 1 × 10−30.

Where it sits Chromosome 16, band 16p13.11 — in an intron of ABCC1.

What each result means

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

Questions about rs2062541

What is rs2062541?

rs2062541 is a single position in the genome, in or near the ABCC1 gene. Published research associates it with phenylalanylphenylalanine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2062541 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 rs2062541 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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Phenylalanylphenylalanine levels (rs2062541). MyGeneLog™. https://www.mygenelog.com/variants/rs2062541

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