ClinVar Miner

List of variants studied for Autosomal recessive nonsyndromic hearing loss 22 by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_144672.4(OTOA):c.2229C>T (p.Ala743=)	rs461179	0.10607
NM_144672.4(OTOA):c.2238G>A (p.Thr746=)	rs72640475	0.01270
NM_144672.4(OTOA):c.1105-17G>A	rs73549643	0.01168
NM_144672.4(OTOA):c.121-20G>A	rs7187792	0.00516

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