Fig. 3

Comparison of allele frequency of pathogenic and likely pathogenic variants in the IndiGen population with the gnomAD, 1000 genome project (1KG), Esp6500, Greater Middle East (GME), and Qatar (Q) and its subpopulation: Amish (AMI), European (Finnish) (EUR (Fin)),, European (Non Finnish) (EUR (Non Fin)), African (AFR), Ashkenazi Jewish (ASJ), East Asian (EAS), South Asian (SAS), American (AMR), Bedouin (BED), Sub-Saharan African (SAF), European (EUR), South Asian (SOU), African Pygmy (APY), Arab (ARA), Persian (PER), Northwest Africa (NWA), Northeast Africa (NEA), Turkish Peninsula (TP), Syrian Desert (SD), Arabian Peninsula (AP), and Persia and Pakistan (PP). CA, Central Asia. Significant allele frequency highlighted with the red circle