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A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki disease
- Source :
- Journal of human genetics. 62(12)
- Publication Year :
- 2017
-
Abstract
- Kawasaki disease (KD), a systemic vasculitis of infants and children, manifests as fever and mucocutaneous inflammation. Although its etiology is largely unknown, the epidemiological data suggest that genetic factors are important in KD susceptibility. To identify genetic variants influencing KD susceptibility, we performed a genome-wide association study (GWAS) and replication study using a total of 915 children with KD and 4553 controls in the Korean population. Six single-nucleotide polymorphisms (SNPs) in three loci were associated significantly with KD susceptibility (P
- Subjects :
- 0301 basic medicine
Genotype
Genome-wide association study
Single-nucleotide polymorphism
Locus (genetics)
Human leukocyte antigen
030204 cardiovascular system & hematology
Biology
Mucocutaneous Lymph Node Syndrome
Polymorphism, Single Nucleotide
Pathogenesis
03 medical and health sciences
0302 clinical medicine
Republic of Korea
Genetics
medicine
Odds Ratio
SNP
Humans
Genetic Predisposition to Disease
Nicotinamide-Nucleotide Adenylyltransferase
Child
Genetics (clinical)
HCP5
Histocompatibility Antigens Class I
medicine.disease
Nucleoside-Triphosphatase
030104 developmental biology
Genetic Loci
Immunology
Kawasaki disease
RNA, Long Noncoding
Genome-Wide Association Study
Subjects
Details
- ISSN :
- 1435232X
- Volume :
- 62
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- Journal of human genetics
- Accession number :
- edsair.doi.dedup.....d8b024739254ac2ee59c2384d7bcc256