LCAT and inherited lipid metabolism disorder: At position 89 of LCAT exon 1, A is substituted for G in 12.5% (5/40) of the sampled population while 87.5% (35/40) of the sampled population retained the G. This G → A SNP was not significantly associated with dyslipidaemia outcomes in HIV-infected individuals on HAART (p = 0.342).