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Lactosyl-N-palmitoyl-sphingosine levels

SLCO5A1 · rs7844108

What the study found

Who was studied 14,296 European ancestry individuals; replicated in 5,698 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0813 lower (95% confidence interval 0.061-0.101); p = 3 × 10−15.

How common The A allele had a frequency of about 52% in the people studied.

Where it sits Chromosome 8, band 8q13.3 — in an intron of SLCO5A1.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Lactosyl-N-palmitoyl-sphingosine levels compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Lactosyl-N-palmitoyl-sphingosine levels.
G/G Published research associates this genotype with typical/baseline likelihood of Lactosyl-N-palmitoyl-sphingosine levels — no copies of the reported risk allele.
Source

Questions about rs7844108

What is rs7844108?

rs7844108 is a single position in the genome, in or near the SLCO5A1 gene. Published research associates it with lactosyl-n-palmitoyl-sphingosine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7844108 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 rs7844108 come from?

GWAS Catalog, Nature medicine 2022, PMID:36357675. 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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Lactosyl-N-palmitoyl-sphingosine levels (rs7844108). MyGeneLog™. https://www.mygenelog.com/variants/rs7844108

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