Sensitive

diarrhoeal disease at age 1 with doctor diagnosis

FUT2 · rs35106244

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

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

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

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

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

Questions about rs35106244

What is rs35106244?

rs35106244 is a single position in the genome, in or near the FUT2 gene. Published research associates it with diarrhoeal disease at age 1 with doctor diagnosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs35106244 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 rs35106244 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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