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Persistent hepatitis B virus infection

INTS10 · rs7000921

Where this position leads

Condition: Chronic Hepatitis B

rs7000921 Condition: Chronic Hepatitis B Chronic Hepatitis B Condition rs7000921 rs7000921 INTS10

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Persistent hepatitis B virus infection compared to the general population. (GWAS Catalog, Nat Commun 2016, PMID:27244555)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Persistent hepatitis B virus infection. (GWAS Catalog, Nat Commun 2016, PMID:27244555)
T/T Published research associates this genotype with typical/baseline likelihood of Persistent hepatitis B virus infection — no copies of the reported risk allele. (GWAS Catalog, Nat Commun 2016, PMID:27244555)

Source: GWAS Catalog, Nat Commun 2016, PMID:27244555

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 rs7000921

What is rs7000921?

rs7000921 is a single position in the genome, in or near the INTS10 gene. Published research associates it with persistent hepatitis b virus infection. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7000921 linked to?

On MyGeneLog this position is linked to Chronic Hepatitis B. The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs7000921?

Subjects that appear in the title or abstract of the same papers as this rsID include infection and immunity (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs7000921 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 rs7000921 come from?

GWAS Catalog, Nat Commun 2016, PMID:27244555. 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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