Table 2 of Chen, Mol Vis 2016; 22:528-535.

Table 2. LTBP2 polymorphisms identified from patients with primary congenital glaucoma.

SNP ID Exon Sequence change Amino acid change Minor allele frequency (%) P value
Affected Unaffected
rs2304707 4 c.956C>A p. Pro319Gln 35/370 (9.5) 7/90 (7.8) 0.62
rs45468895 24 c.3611C>T p. Ala1204Val 1/428 (0.2) 0/200 (0.0) 0.49
rs116914994 29 c.4286G>A p. Arg1429Gln 22/428 (5.1) 16/200 (8.0) 0.16
rs763035721 36 c.5380G>A p. Glu1794Lys 1/428 (0.2) 0/200 (0.0) 0.49

Fisher’s exact test was used to compare the allele frequencies of the LTBP2 variants between PCG patients and controls. A Bonferroni corrected p value of 0.0125 was considered significant.

Chen, Mol Vis 2016; 22:528-535. http://www.molvis.org/molvis/v22/528

©2016 Molecular Vision http://www.molvis.org/molvis/

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