Fig. 1From: Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest ChinaBiochemical analysis of SNP sites in FLT4 and HYDIN genes. (A): Linkage disequilibrium analysis of SNPs in the FLT4 gene: The value shown in the haplotype block diagram is D’, and rs383985 is located at the position of block 198. (B): An enlarged view of the linkage region, which is located in exons 4–8 of the FLT4. (C): The rs1774266 protein function prediction of the HYDIN gene. The mutation is located at the 2042 point of the protein structure (the beginning of the Hydin Adenylate kinase-like domain), and the amino acid is changed from histidine to glutamine. (D): Conservation analysis of the rs1774266 protein sequence, the arrow is the rs1774266 positionBack to article page