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SIFT and PolyPhen-2 were utilized to predict the practical results of the SNPs detected. The protein amounts of CCS in lens-capsule specimens were assessed by Western blotting. The plasma degree of the CCS necessary protein had been assessed utilizing an enzyme-linked immunosorbent assay. OUTCOMES Two coding SNPs (rs1048661 and rs3825942) in LOXL1 gene and a non-synonymous risk variant in CCS gene CCS (c.717CG, p.Asn239Lys) were significantly involving PEXC. The TT genotype of r
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