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Hepatocyte growth factor-like protein levels

PFKFB4 · rs73831580

What the study found

Who was studied 2,935 Qatari ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.415 higher (95% confidence interval 0.33-0.5); p = 3 × 10−20.

How common The G allele had a frequency of about 10% in the people studied.

Where it sits Chromosome 3, band 3p21.31 — in an intron of PFKFB4.

What each result means

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

Questions about rs73831580

What is rs73831580?

rs73831580 is a single position in the genome, in or near the PFKFB4 gene. Published research associates it with hepatocyte growth factor-like protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs73831580 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 rs73831580 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-like protein levels (rs73831580). MyGeneLog™. https://www.mygenelog.com/variants/rs73831580

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