approaching significanceP = 0.06
PGLYRP4 exon 2, c.37A>C Ile13Leu, exon 6 c.575G>T Gly188Val, and exon 9, c.*416A>C, UTR variants may associate with CD or with gender in CD patients PGLYRP4 exon 2, c.37A>C, Ile13Leu (SNP rs30006458), was differentially distributed in CD females compared with CD males and the AA genotype was approaching significance ( P = 0.06, Table S16 ).