Variants in <i>F13A1</i>, <i>F13B</i>, <i>CTLA4</i>, <i>HLA-DRB1</i>, and <i>HLA-DQB1</i> in autoimmune FXIII deficiency cases and its allelic frequency compared with that registered in five databases concerning total and (East) Asia.

When the OR of autoimmune FXIII deficiency against each (East) Asia database was > 1.5 or < 0.67, the OR was represented in bold letters. When the P-value was < 1.00E-8, the value was represented as "<1.00E-8" with a bold letter. Following three cases, chromosome number (Chr), position (Pos), reference nucleotide sequence (Ref), variant nucleotide sequence (Var), and gene ID (Gene ID) were represented in bold letters when the codon mutation type was single AA change. 1) In the case of the OR of autoimmune FXIII deficiency in each database was > 1.5 or < 0.67 no defect was present in all databases. 2) In the case of the OR of autoimmune FXIII deficiency to the non-defective database was all > 1.5 or < 0.67 when there were some defects. 3) In the case of all databases were missing. (XLSX)