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Total cholesterol levels

FAM117B · rs72926986

What the study found

Who was studied 215,551 European ancestry individuals, 57,332 African American individuals, 24,743 Hispanic individuals; replicated in Up to 319,677 individuals.

The effect Each copy of the T allele shifted the measure 0.0326 mg dl-1 lower (95% confidence interval 0.027-0.038); p = 2 × 10−27.

How common The T allele had a frequency of about 28% in the people studied.

Where it sits Chromosome 2, band 2q33.2 — in an intron of FAM117B.

What each result means

G/G No copy of the version the research linked to Total cholesterol levels. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Total cholesterol levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Total cholesterol levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs72926986

What is rs72926986?

rs72926986 is a single position in the genome, in or near the FAM117B gene. Published research associates it with total 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 rs72926986 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 rs72926986 come from?

GWAS Catalog, Nature genetics 2018, PMID:30275531. 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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Total cholesterol levels (rs72926986). MyGeneLog™. https://www.mygenelog.com/variants/rs72926986

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