ClinVar Miner

List of variants reported as likely pathogenic for Autosomal recessive nonsyndromic hearing loss 84B by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378609.3(OTOGL):c.3213+1G>A	rs370730786	0.00004
NM_001378609.3(OTOGL):c.63del (p.Leu22fs)	rs376104832	0.00004
NM_001378609.3(OTOGL):c.1890-1G>T	rs777911261	0.00001

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