Standard

Triglycerides

APOB · rs1042034

Where this position leads

Condition: High Triglycerides

rs1042034 Condition: High Triglycerides High Triglycerides Condition rs1042034 rs1042034 APOB

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Triglycerides compared to the general population. (GWAS Catalog, Nature 2010, PMID:20686565)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Triglycerides. (GWAS Catalog, Nature 2010, PMID:20686565)
T/T Published research associates this genotype with typical/baseline likelihood of Triglycerides — no copies of the reported risk allele. (GWAS Catalog, Nature 2010, PMID:20686565)

Source: GWAS Catalog, Nature 2010, PMID:20686565

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 rs1042034

What is rs1042034?

rs1042034 is a single position in the genome, in or near the APOB gene. Published research associates it with triglycerides. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1042034 linked to?

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

What do people read about alongside rs1042034?

Subjects that appear in the title or abstract of the same papers as this rsID include infection and immunity (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 rs1042034 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 rs1042034 come from?

GWAS Catalog, Nature 2010, PMID:20686565. 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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