ClinVar Miner

List of variants studied for Autosomal recessive nonsyndromic hearing loss 3 by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_016239.4(MYO15A):c.9754A>G (p.Asn3252Asp) rs147458358 0.00177
NM_016239.4(MYO15A):c.2116G>A (p.Ala706Thr) rs932191004 0.00017
NM_016239.4(MYO15A):c.7313dup (p.Glu2439fs)

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