Skip to main content
. 2023 Feb 9;14:1094175. doi: 10.3389/fimmu.2023.1094175

Table 1.

Descriptive information on the TNFRSF1A variants analyzed in the study and their associations with inflammatory markers and disease outcomes.

Instrumental variables rs1800693 a rs767455 b rs4149570 b rs4149577 b
Frequency of EA c 0.574 0.571 0.374 0.528
F-statistic 118.805 98.010 54.020 81.996
Associations with the inflammatory marker, β (SE), p-value
C-reactive protein 0.022 (0.002), 9.56e-27 0.020 (0.002), 2.39e-22 0.015 (0.002), 5.23e-13 0.018 (0.002), 9.60e-19
Associations with the outcome, β (SE), p-value
Periodontitis 0.010 (0.016), 0.530 0.013 (0.016), 0.405 0.004 (0.016), 0.799 0.006 (0.015), 0.685

EA, effect allele; NEA, non-effect allele.

a

SNP used in our primary analysis for the Wald ratio estimation.

b

SNPs used in our secondary analysis for causal estimation from the multiplicative fixed-effects model and the principle component analysis method.

c

Based on allele frequency reported by the genome-wide association studies of C-reactive protein. Single nucleotide polymorphisms were labeled with respect to GRCh37 reference coordinates.