Table 2. ABCB1 SNVs Associated With pCIA in the Discovery Cohort Using Logistic Regression Analysis.

SNV	CHR	Base pair	A1	OR (95% CI)	P valuea	R2b	Source
rs1202179	7	87204279	C	3.79 (2.17-6.62)	3.05 × 10−6	0.98	Genotyped
rs1989831	7	87205479	T	4.01 (2.24-7.17)	2.87 × 10−6	0.98	Imputed
rs1989830	7	87205663	A	3.79 (2.17-6.62)	3.05 × 10−6	0.99	Genotyped
rs1989829	7	87205707	T	3.79 (2.17-6.62)	3.05 × 10−6	0.99	Imputed
rs1202177	7	87207914	C	3.79 (2.17-6.62)	3.05 × 10−6	0.99	Imputed
rs1202176	7	87208987	G	3.79 (2.17-6.62)	3.05 × 10−6	0.99	Imputed
rs1202175	7	87209150	G	3.79 (2.17-6.62)	3.05 × 10−6	0.99	Genotyped
rs1202174	7	87209372	T	3.79 (2.17-6.62)	3.05 × 10−6	0.99	Imputed
rs1202173	7	87210259	A	3.79 (2.17-6.62)	3.05 × 10−6	1	Imputed
rs1202172	7	87210974	C	3.79 (2.17-6.62)	3.05 × 10−6	1	Imputed
rs1202171	7	87211045	T	3.79 (2.17-6.62)	3.05 × 10−6	1	Genotyped
rs1202186	7	87213258	C	3.79 (2.17-6.62)	3.05 × 10−6	1	Genotyped
rs1202185	7	87213384	C	3.79 (2.17-6.62)	3.05 × 10−6	1	Genotyped
rs1202182	7	87215304	G	3.79 (2.17-6.62)	3.05 × 10−6	1	Genotyped
rs1202181	7	87216150	G	3.79 (2.17-6.62)	3.05 × 10−6	1	Genotyped
rs1202180	7	87203840	C	3.57 (2.06-6.19)	5.49 × 10−6	0.97	Imputed
rs1209054	7	87208225	A	3.91 (2.23-6.84)	1.86 × 10−6	0.96	Imputed
rs1211151	7	87208255	T	3.79 (2.17-6.62)	3.05 × 10−6	0.98	Imputed
rs28381820	7	87216216	AAG	3.79 (2.17-6.62)	3.05 × 10−6	0.94	Imputed

Abbreviations: A1, allele 1, effect allele; CHR, chromosome; OR, per-allele odds ratio associated with effect allele; pCIA, persistent chemotherapy-induced alopecia; SNV, single-nucleotide variation.

^aObtained in logistic regression analysis.

^bPairwise correlation between the SNV (R²) and rs1202186.