Variants of genes associated with GO terms “T cell activation,” “antigen presentation,” or “immune tolerance” in autoimmune FXIII deficiency cases.

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 to each database was > 1.5 or < 0.67 when there was no defect in all databases. 2) In the case of the OR of autoimmune FXIII deficiency to the non-defective database was > 1.5 or < 0.67 when there were some defects. 3) In the case of all databases were missing. Polymorphisms that do not have a second (Var2) or third variant (Var3) in autoimmune FXIII deficiency are displayed in a gray box.
(XLSX)