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Article Abstract

To identify novel host genetic variants that predispose to hepatitis B virus (HBV) persistence, we performed the first genome-wide association study in the Thai population involving 318 cases of chronic hepatitis B and 309 healthy controls after quality control measures. We detected the genome-wide significant association of the class II region (, rs7770370, -value = 7.71 × 10, OR = 0.49) with HBV chronicity. Subsequent allele imputation revealed ( = 1.21 × 10, OR = 0.53), ( = 2.17 × 10, OR = 0.50), and ( = 2.17 × 10, OR = 0.07) as protective alleles, and ( = 6.32 × 10, OR = 1.63), ( = 1.13 × 10, OR = 1.72), ( = 4.68 × 10, OR = 1.60), and ( = 1.11 × 10, OR = 1.84) as risk alleles for HBV persistence. We also detected suggestive associations in the (rs35766154), (rs62321986), (rs144998273), and (rs1828682) loci. Among single-nucleotide polymorphisms in the locus, rs1061307 was identified as the primary functional variant by functional analysis. In addition to replicating the association of the class II region, we detected novel candidate loci that provide new insights into the pathophysiology of chronic hepatitis B.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234442PMC
http://dx.doi.org/10.3389/fgene.2022.887121DOI Listing

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