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Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels

near CBX4 · rs139679715

What the study found

Who was studied 2,935 Qatari ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.65 higher (95% confidence interval 0.5-0.8); p = 5 × 10−17.

How common The A allele had a frequency of about 3% in the people studied.

Where it sits Chromosome 17, band 17q25.3 — between genes, 16.9 kb from CBX4.

What each result means

A/A Two copies of the version the research linked to Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 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 Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels. This is the starting point the study compared everyone against.
Source

Questions about rs139679715

What is rs139679715?

rs139679715 is a single position in the genome, in or near the near CBX4 gene. Published research associates it with ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs139679715 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 rs139679715 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.

Quoting this page

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Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels (rs139679715). MyGeneLog™. https://www.mygenelog.com/variants/rs139679715

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