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. Author manuscript; available in PMC: 2021 Mar 1.
Published in final edited form as: Pain. 2020 Mar;161(3):619–629. doi: 10.1097/j.pain.0000000000001750

Table 1.

SNPs selected for the genetic association analysis.

Gene or metabolic pathway rs number Location Functional change Gene symbol Gene name Reference
OPRM1 gene rs1799971 Exon 1 Asn40Asp OPRM1 Opioid Receptor Mu 1 [4,810,24,27,35,44,49]

COMT gene rs6269 Intron 2 COMT Catechol-O-Methyl Transferase [14,43,59,82]
rs4633 Codon 62
rs4818 Exon 4
rs4680 Exon 4 Val158Met

Serotonin receptor rs6313 Exon 2 T102C HTR2A 5-Hydroxytryptamine Receptor 2A [28,45,77,94]
rs7997012 13:46837850

ABCB1 gene rs1045642 Exon 26 C3435T ABCB1 ATP Binding Cassette Subfamily B [33,36,65]
rs2032582 Exon 21 Ala893Thr Member 1

CYP2C19 metabolism rs12248560 Promoter CYP2C19 Cytochrome P450 Family 2 [25,30,31,71,80]
rs4244285 Exon 5 Subfamily C Member 19
rs4986893 Exon 4
rs28399504 Exon 1
rs56337013 Exon 9
rs72552267 Exon 3
rs72558186 Intron 5
rs41291556 Exon 3

CYP2D6 metabolism rs1065852 22:42130692 P34S CYP2D6 Cytochrome P450 Family 2 [25,30,31,80]
rs201377835 22:42129910 Subfamily D Member 6
rs5030862 22:42130668 G42R
rs72549357 22:42526657
rs28371706 22:42129770 T107I
rs1080985 22:42132375
rs72549354 22:42128815
rs59421388 22:42127608 V338M
rs35742686 22:42128242 259Frameshift
rs769258 22:42130761
rs3892097 22:42128945 Splicing defect
rs28371725 Intron 6 Splicing defect
rs1135840 22:42126611 S486T
rs5030655 22:42129084 118Frameshift
rs5030867 22:42127856 H324P
rs5030865 22:42129033 G169R
rs5030656 22:42128174 K281del