Association between inherited monogenic liver disorders and chronic hepatitis C

Table 1 Genotyping methods used in the present study

Disease	Gene	Mutation	rs1	Analysis method
Hereditary hemochromatosis	HFE	C282Y	rs1800562	PCR-RFLP with restrictase RsaI[18]
		H63D	rs1799945	PCR-RFLP with restrictase MboI[18]
Gilbert’s syndrome	UGT1A1	(TA)7, UGT1A1*28	rs8175347	Fluorescent PCR[20]
Alpha-1 antitrypsin deficiency	SERPINA1	PIZ	rs28929474	Bi-PASA[19]
Wilson’s disease	ATP7B	H1069Q	rs76151636	Bi-PASA[4]

¹Single nucleotide polymorphism database number (http://www.ncbi.nlm.nih.gov/snp/). PCR: Polymerase chain reaction; RFLP: Restriction fragment length polymorphism analysis; Bi-PASA: Bidirectional PCR allele-specific amplification.