Standard

Chronic hepatitis C infection

IL29 · rs8099917

What each result means

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Chronic hepatitis C infection compared to the general population. (GWAS Catalog, Gastroenterology 2010, PMID:20060832)
G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Chronic hepatitis C infection. (GWAS Catalog, Gastroenterology 2010, PMID:20060832)
T/T Published research associates this genotype with typical/baseline likelihood of Chronic hepatitis C infection — no copies of the reported risk allele. (GWAS Catalog, Gastroenterology 2010, PMID:20060832)

Source: GWAS Catalog, Gastroenterology 2010, PMID:20060832

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs8099917

What is rs8099917?

rs8099917 is a single position in the genome, in or near the IL29 gene. Published research associates it with chronic hepatitis c infection. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What do people read about alongside rs8099917?

Subjects that appear in the title or abstract of the same papers as this rsID include alcohol and the flush (1 papers), exercise and muscle (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs8099917 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 rs8099917 come from?

GWAS Catalog, Gastroenterology 2010, PMID:20060832. 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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