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Hepatocyte growth factor activator levels

DOK7 · rs62275879

What the study found

Who was studied 2,935 Qatari ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.95 lower (95% confidence interval 0.71-1.19); p = 3 × 10−15.

How common The T allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 4, band 4p16.3 — in an intron of DOK7.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Hepatocyte growth factor activator levels — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Hepatocyte growth factor activator levels.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Hepatocyte growth factor activator levels compared to the general population.
Source

Questions about rs62275879

What is rs62275879?

rs62275879 is a single position in the genome, in or near the DOK7 gene. Published research associates it with hepatocyte growth factor activator levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs62275879 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 rs62275879 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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Hepatocyte growth factor activator levels (rs62275879). MyGeneLog™. https://www.mygenelog.com/variants/rs62275879

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