Table 2 Association summary of the lead genetic variant

From: Common and rare genetic variants predisposing females to unexplained recurrent pregnancy loss

     

Risk allele frequency

  

rsID

Chr

Position

(hg19)

Alleles

Risk

Allele

Case

Control

OR (95% CI)

P-value

rs9263738

6

31,109,767

T/C

T

0.893

0.871

1.51 (1.33–1.72)

1.4 × 10−10

  1. Two-sided association testing was performed using SAIGE. The P-value is unadjusted for multiple comparisons.
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