ClinVar Miner

List of variants studied for Autosomal recessive nonsyndromic hearing loss 3 by GenomeConnect, ClinGen

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.3385C>T (p.Arg1129Ter)	rs748868741	0.00002
NM_016239.4(MYO15A):c.9765_9766insGG (p.Ile3256fs)	rs757070287	0.00001
NM_016239.4(MYO15A):c.1661dup (p.Leu555fs)	rs1245338270
NM_016239.4(MYO15A):c.7124_7127del (p.Asp2375fs)	rs780170125

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