highly significantp < 0.01
Verification analysis results show that the mutation sites of CCSER1 (snp12579,34,449,796, A → G), RPS6KC1 (snp41503,69,173,527, A → G), KCNRG (snp41082, 67,134,820, G → A), KCNK9 (14: 78472665,78,472,665, G → A), and CLYBL (12: 9705753,9,705,753, C → T) were consistent with the results of GWAS analysis and highly significant ( p < 0.01).