We selected five of the most significant SNPs (rs7572473, rs12473679, rs17529497, rs7605378, and rs10203122) of FTCDNL1 based on a previous study with a minimum allele frequency of ≥ 1% in a Beijing Han Chinese population[17 (link)]. The FTCDNL1 gene structure is shown in Fig 1. Genotyping was performed by the TaqMan Allelic Discrimination assay (Applied Biosystems, Foster City, CA). The polymerase chain reaction (PCR) was accomplished by an ABI StepOnePlus Thermal Cycler. In a subsequent PCR, the fluorescence from specific probes was detected and analyzed through the System SDS software version 2.2.2 (Applied Biosystems).
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