Standard

Low density lipoprotein cholesterol levels

CERT1 · rs116070404

What the study found

Who was studied 341,875 European ancestry individuals, 6,003 African ancestry individuals, 7,319 South Asian ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0335 lower (95% confidence interval 0.023-0.044); p = 4 × 10−10.

Where it sits Chromosome 5, band 5q13.3 — in an intron of CERT1.

What each result means

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

Questions about rs116070404

What is rs116070404?

rs116070404 is a single position in the genome, in or near the CERT1 gene. Published research associates it with low density lipoprotein cholesterol levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs116070404 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 rs116070404 come from?

GWAS Catalog, Nature genetics 2021, PMID:33462484. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Low density lipoprotein cholesterol levels (rs116070404). MyGeneLog™. https://www.mygenelog.com/variants/rs116070404

← See all variants