CTNNA3 genetic polymorphism may be a new genetic signal of type 2 diabetes in the Chinese Han population: a case control study

Table 2 The basic information and HWE about the selected SNPs of CTNNA3

Gene	SNP ID	Function	Chr: position	Alleles (A/B)	MAF		HWE (P value)	Haploreg 4.1
Gene	SNP ID	Function	Chr: position	Alleles (A/B)	Cases	Controls	HWE (P value)	Haploreg 4.1
CTNNA3	rs10822745	Intronic	10: 66,194,307	C/T	0.429	0.417	0.646	Motifs changed
CTNNA3	rs7920624	Intronic	10: 66,203,428	A/T	0.488	0.498	0.929	Motifs changed
CTNNA3	rs2441727	Intronic	10: 66,465,128	A/G	0.182	0.204	0.406	NHGRI/EBI GWAS hits
CTNNA3	rs7914287	Intronic	10: 67,590,805	T/C	0.355	0.292	0.124	–

HWE, Hardy–Weinberg equilibrium; Alleles (A/B), minor/major allele; SNP, single nucleotide polymorphisms; MAF, minor allele frequency
p > 0.05 indicates that the genotypes were in Hardy–Weinberg Equilibrium

ISSN: 1755-8794