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Comparison of Indian allele frequencies of clinically relevant PGx variants with populations in 1000 Genomes dataset, gnomAD database, GME database and Qatar database. PGx variants in Indians which yielded significant p-value (p < 0.05) in the Fisher’s exact test comparing Indian allele frequency with other databases are highlighted in green outer circle.
GME: Greater Middle East; PGx: Pharmacogenetic.
