Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India - Narang, Ankita; Uppilli, Bharathram; Vivekanand, Asokachandran; Naushin, Salwa; Yadav, Arti; Singhal, Khushboo; Shamim, Uzma; Sharma, Pooja; Zahra, Sana; Mathur, Aradhana; Seth, Malika; Parveen, Shaista; et al. (Human mutation, 2020)
Keywords: ClinVar variants; Diabetes mellitus; Genetic screening; Genotypes; Genotyping; high‐throughput genotyping; Inborn errors of metabolism; Indian populations; monogenic diseases; Phenotypes; database; ClinVar variants; Indian populations; high-throughput genotyping; monogenic diseases