Review Article

Human L-Ficolin (Ficolin-2) and Its Clinical Significance

Table 2

Potentially important polymorphisms in the FCN2 gene.

SNP no.Region and positionBase substitutionAmino acid substitution

rs3124952promoter −986A>G
rs3124953promoter −602G>A
rs3811140promoter −557A>G
rs28969369promoter −64A>C
rs17514136promoter −4A>G
rs17549193exon 8 +6359C>TThr236Met
rs7851696exon 8 +6424G>TAla258Ser