Standard

Body mass index

LINC00558 · rs1379828

Where this position leads

Condition: Childhood Body Mass Index

rs1379828 Condition: Childhood Body Mass Index Childhood Body Mass Index Condition rs1379828 rs1379828 LINC00558

What the study found

Who was studied 441,761 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.017 higher (95% confidence interval 0.012-0.022); p = 1 × 10−12.

Where it sits Chromosome 13, band 13q14.3 — inside LINC00558.

What each result means

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

Questions about rs1379828

What is rs1379828?

rs1379828 is a single position in the genome, in or near the LINC00558 gene. Published research associates it with body mass index. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1379828 linked to?

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

Does having rs1379828 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 rs1379828 come from?

GWAS Catalog, Diabetologia 2023, PMID:37280435. 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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Body mass index (rs1379828). MyGeneLog™. https://www.mygenelog.com/variants/rs1379828

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