5mL of peripheral venous blood were collected from each subject. Then, the genomic DNA was extracted using the standard phenol-chloroform method for genotyping. SNPs were selected based on positive reported variants for obesity from previous GWAS studies.13 (link)–15 (link),18 (link) Six SNPs (rs6499640, rs1421085, rs8050136, rs3751812, rs9939609 and rs9930506) were genotyped in this study. Among them, all these six SNPs were successfully genotyped by matrix-assisted laser desorption/ionization time of flight (MALDI-TOF) mass spectrometry using the MassARRAY® Analyzer 4 platform (Sequenom, San Diego, CA). The probes and primers were designed using Mysequenom online software with the accompanying Assay Design Suite v2.0. The standard polymerase chain reaction (PCR) was performed in a total volume of 5 μL containing 10 ng of genomic DNA. Detailed information regarding the primers and PCR reaction conditions is available on request.