"Baylor Genetics"[submitter] AND "OTOGL"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 501971	NM_001378609.3(OTOGL):c.1395-3T>C	OTOGL	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 84B +1 more	GUncertain significance
Select item 505143	NM_001378609.3(OTOGL):c.3277A>C (p.Asn1093His)	OTOGL (N1084H +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 500879	NM_001378609.3(OTOGL):c.3488A>G (p.Asp1163Gly)	OTOGL (D1154G +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 504850	NM_001378609.3(OTOGL):c.3566A>G (p.Gln1189Arg)	OTOGL (Q1180R +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1031268	NM_001378609.3(OTOGL):c.3626A>G (p.Tyr1209Cys)	OTOGL (Y1164C +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 84B	GUncertain significance
Select item 1031269	NM_001378609.3(OTOGL):c.3931C>T (p.His1311Tyr)	OTOGL (H1266Y +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 84B	GUncertain significance
Select item 504927	NM_001378609.3(OTOGL):c.4234A>G (p.Met1412Val)	OTOGL (M1403V +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity

ClinVar