Sensitive

diarrhoeal disease at age 1

NTN5 · rs8111874

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of diarrhoeal disease at age 1 — no copies of the reported risk allele. (GWAS Catalog, Hum Mol Genet 2016, PMID:27559109)

A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with diarrhoeal disease at age 1. (GWAS Catalog, Hum Mol Genet 2016, PMID:27559109)

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of diarrhoeal disease at age 1 compared to the general population. (GWAS Catalog, Hum Mol Genet 2016, PMID:27559109)

Source: GWAS Catalog, Hum Mol Genet 2016, PMID:27559109

Questions about rs8111874

What is rs8111874?

rs8111874 is a single position in the genome, in or near the NTN5 gene. Published research associates it with diarrhoeal disease at age 1. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs8111874 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 rs8111874 come from?

GWAS Catalog, Hum Mol Genet 2016, PMID:27559109. 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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