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Phospholipids to total lipids in IDL percentage (UKB data field 23609)

MACF1 · rs66880209

What the study found

Who was studied 88,329 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0408 higher (95% confidence interval 0.028-0.053); p = 2 × 10−10.

How common The A allele had a frequency of about 16% in the people studied.

Where it sits Chromosome 1, band 1p34.3 — inside MACF1.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Phospholipids to total lipids in IDL percentage (UKB data field 23609) compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Phospholipids to total lipids in IDL percentage (UKB data field 23609).
G/G Published research associates this genotype with typical/baseline likelihood of Phospholipids to total lipids in IDL percentage (UKB data field 23609) — no copies of the reported risk allele.
Source

Questions about rs66880209

What is rs66880209?

rs66880209 is a single position in the genome, in or near the MACF1 gene. Published research associates it with phospholipids to total lipids in idl percentage (ukb data field 23609). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs66880209 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 rs66880209 come from?

GWAS Catalog, Biological psychiatry 2023, PMID:36764567. 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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Phospholipids to total lipids in IDL percentage (UKB data field 23609) (rs66880209). MyGeneLog™. https://www.mygenelog.com/variants/rs66880209

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