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. 2021 Jun 29;12:685524. doi: 10.3389/fendo.2021.685524

Table 2.

Significant results for single marker based association analyses.

CHR SNP A1 Genotypic Analysis Allelic Analysis *P
Genotypes Patients Controls OR[95% CI] χ2 P Alleles Patients Controls OR[95% CI] χ2 P
6 rs80196932 C CC 15 65 0.50[0.28-0.87]
CT 262 748 0.75[0.64-0.88] C 292 878 0.74[0.64-0.85]
TT 1,005 2,155 ref 17.53 0.0002 T 2,272 5,058 ref 17.47 2.93×10-5 2.79×10-5
16 rs117267808 A AA 9 9 2.44[0.97-6.18]
AG 218 380 1.40[1.17-1.68] A 236 398 1.41[1.19-1.67]
GG 1,055 2,579 ref 16.81 0.0002 G 2,328 5,538 ref 16.21 5.68×10-5 6.20×10-5

CHR, chromosome; A1, tested allele (minor allele); OR [95%CI], odds ratio with 95% confidence interval.

Threshold for P-Value was 0.05/20 = 0.0025.

*P values after being adjusted for age and prepregnancy BMI using logistic models.