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Glutamyl aminopeptidase levels

PANCR · rs3796879

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.201 higher (95% confidence interval 0.15-0.25); p = 6 × 10−17.

How common The T allele had a frequency of about 8% in the people studied.

Where it sits Chromosome 4, band 4q25 — in an intron of PANCR.

What each result means

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

Questions about rs3796879

What is rs3796879?

rs3796879 is a single position in the genome, in or near the PANCR gene. Published research associates it with glutamyl aminopeptidase levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs3796879 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 rs3796879 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. 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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Glutamyl aminopeptidase levels (rs3796879). MyGeneLog™. https://www.mygenelog.com/variants/rs3796879

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