Carriers of Rare Missense Variants in IFIH1 Are Protected from Psoriasis View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2010-12

AUTHORS

Yonghong Li, Wilson Liao, Michele Cargill, Monica Chang, Nori Matsunami, Bing-Jian Feng, Annie Poon, Kristina P Callis-Duffin, Joseph J Catanese, Anne M Bowcock, Mark F Leppert, Pui-Yan Kwok, Gerald G Krueger, Ann B Begovich

ABSTRACT

Testing of ∼25,000 putative functional single-nucleotide polymorphisms (SNPs) across the human genome in a genetic association study has identified three psoriasis genes, IL12B, IL23R, and IL13. We now report evidence for the association of psoriasis risk with missense SNPs in the interferon induced with helicase C domain 1 gene (IFIH1). The rare alleles of two independent SNPs were associated with decreased risk of psoriasis--rs35667974 (Ile923Val): odds ratio (OR) for minor allele carriers is 0.43, P=2.36 × 10(-5) (2,098 cases vs. 1,748 controls); and rs10930046 (His460Arg): OR for minor allele carriers is 0.51, P=6.47 × 10(-4) (2,098 cases vs. 1,744 controls). Compared to noncarriers, carriers of the 923Val and/or 460Arg variants were protected from psoriasis (OR=0.46, P=5.56 × 10(-8)). To our knowledge, these results suggest that IFIH1 is a previously unreported psoriasis gene. More... »

PAGES

2768-2772

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/jid.2010.214

DOI

http://dx.doi.org/10.1038/jid.2010.214

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1020225998

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/20668468


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