Table 2.

Characteristics of the 11 polymorphisms studied and genotyping results in the study sample

Gene locus	SNP	Chromosome	Location	Position	Genotype	n	%	MAF
CYP19A1	rs727479	15	Intron 1	49 321 839	AA	40	36.36	0.364
					AC	60	54.55
					CC	10	9.09
CYP19A1	rs1008805	15	Exon 1	49 336 891	AA	27	24.55	0.473
					AG	62	56.36
					GG	21	19.09
CYP19A1	rs749292	15	Exon 1	49 346 023	AA	16	14.55	0.600
					AG	56	50.91
					GG	38	34.55
CYP19A1	rs730154	15	Exon 1	49 378 496	CC	31	28.18	0.368
					CT	77	70.00
					TT	2	1.82
near TCL1A	rs7158782*	14	Intronic	95 238 884	AA	85	77.27	0.118
					AG	24	21.82
					GG	1	0.91
near TCL1A	rs7159713	14	Intronic	95 239 330	AA	84	76.36	0.123
					AG	25	22.73
					GG	1	0.91
near TCL1A	rs2369049	14	Intronic	95 241 604	AA	85	77.27	0.118
					AG	24	21.82
					GG	1	0.91
near TCL1A	rs11849538	14	Intronic	95 245 031	CC	89	80.91	0.100
					CG	20	18.18
					GG	1	0.91
ABCB1	rs1128503 (C1236T)	7	Exon 12	87 550 285	CC	25	22.73	0.495
					CT	61	55.45
					TT	24	21.82
ABCB1	rs2032582 (G2677 T)	7	Exon 21	87 531 302	GG	35	31.82	0.450
					GT	51	46.36
					TT	24	21.82
ABCB1	rs1045642 (C3435T)	7	Exon 26	87 509 329	CC	48	43.64	0.386
					CT	39	35.45
					TT	23	20.91

^* In full linkage disequilibrium with rs2369049; MAF, minor allele frequency; SNP, single‐nucleotide polymorphism