ClinVar Miner

List of variants reported as likely pathogenic for Hearing loss, autosomal recessive by Center for Statistical Genetics, Columbia University

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.6634G>A (p.Glu2212Lys)	rs371352836	0.00001
NM_016239.4(MYO15A):c.9303+5G>A	rs1555547215	0.00001

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