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Liver LILRB5 levels

LILRB5 · rs10405357

What the study found

Who was studied 241 European ancestry individuals.

The effect The reported allele is C; the catalogue records no effect size ; p = 2 × 10−10.

Where it sits Chromosome 19, band 19q13.42 — in an intron of LILRB5.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Liver LILRB5 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 Liver LILRB5 levels.
T/T Published research associates this genotype with typical/baseline likelihood of Liver LILRB5 levels — no copies of the reported risk allele.
Source

Questions about rs10405357

What is rs10405357?

rs10405357 is a single position in the genome, in or near the LILRB5 gene. Published research associates it with liver lilrb5 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10405357 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 rs10405357 come from?

GWAS Catalog, Molecular metabolism 2026, PMID:41456820. 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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Liver LILRB5 levels (rs10405357). MyGeneLog™. https://www.mygenelog.com/variants/rs10405357

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