Standard

Psoriasis

IL23R · rs9988642

Where this position leads

Condition: Psoriasis

rs9988642 Condition: Psoriasis Psoriasis Condition rs9988642 rs9988642 IL23R

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Psoriasis — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Psoriasis.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Psoriasis compared to the general population.
Source

Questions about rs9988642

What is rs9988642?

rs9988642 is a single position in the genome, in or near the IL23R gene. Published research associates it with psoriasis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs9988642 linked to?

On MyGeneLog this position is linked to Psoriasis. The research behind each link, and its sources, are set out on that condition page.

Does having rs9988642 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 rs9988642 come from?

GWAS Catalog, Nat Genet 2012, PMID:23143594. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

← See all variants