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. Author manuscript; available in PMC: 2013 Apr 26.
Published in final edited form as: Pharmacogenet Genomics. 2012 Nov;22(11):784–795. doi: 10.1097/FPC.0b013e3283589a76

Table 3.

The top-associated variants in all drug-induced liver injury casesa for all single-nucleotide polymorphisms and selected subsets of single-nucleotide polymorphisms associated with absorption, distribution, metabolism, and excretion and autoimmune genes

SNP Sets SNP P-value Chromosome:coordinate Function Nearest gene
Genome-wide rs35709459 1.99E – 07 X:91516677 Intronic PCDH11X
rs35925943 1.38E – 06 X:91516339 Intronic PCDH11X
rs11767067 1.64E – 06 7:93022840 Intergenic CALCR
rs1187997 2.18E – 06 1:58455538 Intronic DAB1
rs656437 4.24E – 06 11:95770378 Intronic MAML2
ADME subset rs3740065 0.0001 10:101605693 Intronic ABCC2
rs2756113 0.0008 10:101569371 Intronic ABCC2
rs2804397 0.0011 10:101559415 Intronic ABCC2
rs8187710 0.0013 10:101611294 Missense (C1515Y) ABCC2
rs11816708 0.0013 10:101615015 Downstream ABCC2
Autoimmune subset rs2476601 2.26E – 05 1:114377568 Missense (R620W) PTPN22
rs6679677 4.18E – 05 1:114303808 Upstream RSBN1
rs7202877 0.0002 16:75247245 Intergenic CTRB1
rs1464510 0.003 3:188112554 Intronic LPP
rs12928822 0.0033 16:11403893 Upstream MIR548H2

ADME, absorption, distribution, metabolism, and excretion; SNP, single-nucleotide polymorphism.

a

Analysis conditioned on rs2395029, rs2523822, and rs3135388, known to be highly associated with drug-induced liver injury due to flucloxacillin or amoxicillin/clavulanate.