CFTR and cystic fibrosis: Since the standard 39-variant CFTR panel was more likely to miss CF-causing DNA variants in infants from minoritized groups, particularly those reported as Hispanic, the NYS consortium reached consensus that the NBS program should continue to refer infants in the VHIRT category [27], but eventually raised the cut-off from 0.2% to 0.1%, leading to a large decrease in referrals without missing pancreatic-insufficient infants with CF [26].