ClinVar Miner

List of variants reported as likely pathogenic for autosomal recessive nonsyndromic hearing loss 25

Included ClinVar conditions (1):

Autosomal recessive nonsyndromic hearing loss 25

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001080476.3(GRXCR1):c.469G>T (p.Glu157Ter)	rs774844858	0.00001
NM_001080476.3(GRXCR1):c.79C>T (p.Arg27Ter)	rs769983282	0.00001
NM_001080476.3(GRXCR1):c.668T>A (p.Leu223Gln)

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