ClinVar Miner

List of variants reported as uncertain significance for autosomal recessive nonsyndromic hearing loss 84B by Service de Biologie Medicale, CIUSSS du Saguenay-Lac-Saint-Jean

Included ClinVar conditions (1):

Autosomal recessive nonsyndromic hearing loss 84B

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_001378609.3(OTOGL):c.5050G>A (p.Gly1684Arg)	rs778223464	0.00002

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