UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population

Table 3

Association analysis of identified common variants.

Number	SNP	Coordinate Hg19	Ref	Alt	F_A	F_U	CHISQ	value	OR	CI (low-up)	-value
(1)	rs10929303	234681416	C	T	0.078	0.158	7.0800	0.008	0.4521	0.1946–1.0480	0.062
(2)	rs8330	234681645	C	G	0.078	0.141	4.6710	0.030	0.5172	0.2431–1.3864	0.112
(3)	rs1042640	234681544	C	G	0.078	0.136	4.1270	0.042	0.5360	0.2337–1.3176	0.112
(4)	rs2302538	234676413	T	C	0.091	0.051	2.8120	0.093	1.8590	0.6560–5.3130	0.187
(5)	rs4148323	234669144	G	A	0.078	0.051	1.3960	0.237	1.5710	0.5402–4.6176	0.379

Ref: reference, Alt: alternative, F_A: frequency Alt in cases, and F_U: frequency Alt in controls.