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Ectonucleoside triphosphate diphosphohydrolase 5 levels

LIN52 · rs139569341

What the study found

Who was studied 2,935 Qatari ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.851 lower (95% confidence interval 0.66-1.04); p = 4 × 10−18.

How common The C allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 14, band 14q24.3 — in an intron of LIN52.

What each result means

C/C Two copies of the version the research linked to Ectonucleoside triphosphate diphosphohydrolase 5 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Ectonucleoside triphosphate diphosphohydrolase 5 levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to Ectonucleoside triphosphate diphosphohydrolase 5 levels. This is the starting point the study compared everyone against.
Source

Questions about rs139569341

What is rs139569341?

rs139569341 is a single position in the genome, in or near the LIN52 gene. Published research associates it with ectonucleoside triphosphate diphosphohydrolase 5 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs139569341 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 rs139569341 come from?

GWAS Catalog, Human molecular genetics 2023, PMID:36168886. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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Ectonucleoside triphosphate diphosphohydrolase 5 levels (rs139569341). MyGeneLog™. https://www.mygenelog.com/variants/rs139569341

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