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Table 2 R2 and F-statistic results for the genetic variants that were genome wide significant in the original genome wide association study

From: Maternal plasma cortisol’s effect on offspring birth weight: a Mendelian Randomisation study

Genetic variant (SNP) ID

Number of-participants

Minor allele frequency

Per allele difference (SDs of log-transformed units) in plasma cortisol (95% CI)

R2

F-Statistic

rs11620763

25314

0.19

0.09 (0.06 to 0.11)

0.0023

57.49

rs2736898

25314

0.49

0.06 (0.04 to 0.07)

0.0017

43.37

rs7146221

25314

0.45

0.05 (0.03 to 0.07)

0.0013

31.87

rs9989237a

25314

0.21

0.09 (0.07 to 0.10)

0.0024

61.83

  1. aSNP used in main analysis
  2. bThe R2 and F-statistics for rs11620763, rs2736898 and rs7146221 may be under or overestimated due to linkage disequilibrium with rs9989237