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. 2021 May 11;16(5):e0251289. doi: 10.1371/journal.pone.0251289

Table 2. Candidate gene burden tests comparing the number of variants in CM-1 cases with public controls from gnomAD.

Candidate Gene Number of SNPs passing filtering Fisher exact 1-sided p-value Odds Ratio (OR) Lower Confidence Interval of OR Upper Confidence Interval of OR
PLOD1 2 0.8149 0.794 0.265 1.785
MSGN1 1 +
COL3A1 6 0.2935 1.362 0.633 2.519
COL5A2 12 0.0001 1.814 1.327 2.426
COL7A1 14 0.0006 2.424 1.501 3.69
COL6A5 23 <0.0001 1.99 1.463 2.648
CDX1 0 *
ADAMTS2 5 0.2719 1.198 0.751 1.807
TNXB 48 0.9999 0.228 0.167 0.306
VEGFA 1 +
DSE 4 0.8806 0.757 0.383 1.326
COL1A2 3 0.0095 8.273 2.303 20.678
RDH10 0 *
COL5A1 7 0.0934 1.399 0.895 2.078
NRP1 1 +
VEGFB 3 0.0036 7.436 2.467 16.884
FLT1 8 0.001 3.354 1.752 5.766
HIF1A 4 0.3037 1.509 0.568 3.178
PGF 1 +
ALDH1A2 0 *
COL1A1 4 0.0709 2.532 0.953 5.339

Significant p-values are indicated in bold.

+These genes only contained a single variant that surpassed our quality control filters and thus, were dropped from the burden analysis.

*These genes did not contain variants that surpassed our quality control filters and thus, were dropped from analysis.