The list of the codon mutations that probably cause damage with variant allelic frequency < 0.01 in 20 autoimmune FXIII deficiency cases.

When the allelic frequency of the database was < 1.00E-2, the frequency was represented in bold letters. 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. When the case numbers whose genotypes were “Homozygous” or “Heterozygous” were ≥ 10, chromosome number (Chr), position (Pos), reference nucleotide sequence (Ref), and variant nucleotide sequence (Var) were represented in bold letters.
(XLSX)