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Fig. 5 | BMC Medical Genetics

Fig. 5

From: Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss

Fig. 5

The number of identified variants in different populations. The rank (from high to low) of reported number of MYO15A variants in different populations in the Middle East, Southeast Asia, South Asia, Europe, South America, and North America. This illustrates that in the Middle East and South Asia, most MYO15A variants were homozygous variants. On the other hand, more compound heterozygous variants were identified in Southeast Asia and Europe

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