Regulatory Variants on the Leukocyte Immunoglobulin-Like Receptor Gene Cluster are Associated with Crohn's Disease and Interact with Regulatory Variants for TAP2

Crohn's disease [CD] has a complex polygenic aetiology with high heritability. There is ongoing effort to identify novel variants associated with susceptibility to CD through a genome-wide association study [GWAS] in large Korean populations. Genome-wide variant data from 902 Korean patients wi...

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Veröffentlicht in:	Journal of Crohn's and colitis 2024-01, Vol.18 (1), p.47-53
Hauptverfasser:	Kim, Kwangwoo, Oh, Shin Ju, Lee, Junho, Kwon, Ayeong, Yu, Chae-Yeon, Kim, Sangsoo, Choi, Chang Hwan, Kang, Sang-Bum, Kim, Tae Oh, Park, Dong Il, Lee, Chang Kyun
Format:	Artikel
Sprache:	eng
Schlagworte:	ATP Binding Cassette Transporter, Subfamily B, Member 3 - genetics Case-Control Studies Crohn Disease - genetics Genetic Predisposition to Disease Genome-Wide Association Study Histocompatibility Antigens Class I - genetics Humans Immunoglobulins Multigene Family Polymorphism, Single Nucleotide
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