Table 3 of Firasat, Mol Vis 2008; 14:2002-2009.

Table 3. Single nucleotide polymorphism (SNP) profile of PCG patients from all three families linked to CYP1B1.

Family rs2617266 rs10012 rs1056827 rs1056836 rs1056837 rs1800440
PKGL021 T G T C C A
PKGL022 T G T C C A
PKGL026 C C G G T A

To trace CYP1B1 mutations identified in this study haplotypes for six intragenic SNPs including rs2617266, which is 12 bp upstream of the first coding exon of CYP1B1, rs10012, rs1056827, rs1056836, rs1056837, and rs1800440 were constructed.

Firasat, Mol Vis 2008; 14:2002-2009. http://www.molvis.org/molvis/v14/a236

©2008 Molecular Vision http://www.molvis.org/molvis/

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