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Fig. 2 | BMC Medical Genomics

Fig. 2

From: A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newborns

Fig. 2

A schematic diagram showing the location of primers and hotspot variants. White boxes indicate exons, and the black boxes indicate the coding region. The lines above the coding regions indicate primers. The red lines present the primers in well 1, blue lines present the primers in well 2. The variants were pathogenic variants with an allele frequency greater than 1/10,000 in the gnomAD database

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