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Cleft palate

GRHL3 · rs41268753

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 Cleft palate — no copies of the reported risk allele. (GWAS Catalog, Am J Hum Genet 2016, PMID:27018472)

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Cleft palate. (GWAS Catalog, Am J Hum Genet 2016, PMID:27018472)

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Cleft palate compared to the general population. (GWAS Catalog, Am J Hum Genet 2016, PMID:27018472)

Source: GWAS Catalog, Am J Hum Genet 2016, PMID:27018472

Questions about rs41268753

What is rs41268753?

rs41268753 is a single position in the genome, in or near the GRHL3 gene. Published research associates it with cleft palate. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs41268753 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 rs41268753 come from?

GWAS Catalog, Am J Hum Genet 2016, PMID:27018472. 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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