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

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

Gene SNP ID Function Chr: position Alleles
(A/B)
MAF HWE
(P value)
Haploreg 4.1
Cases Controls
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
  1. HWE, Hardy–Weinberg equilibrium; Alleles (A/B), minor/major allele; SNP, single nucleotide polymorphisms; MAF, minor allele frequency
  2. p > 0.05 indicates that the genotypes were in Hardy–Weinberg Equilibrium