ClinVar Miner

List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 22 by Genomic Research Center, Shahid Beheshti University of Medical Sciences

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_144672.4(OTOA):c.1820C>T (p.Ala607Val)	rs764347046	0.00001
NM_144672.4(OTOA):c.1831T>C (p.Trp611Arg)	rs1567391195

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