"Baylor Genetics"[submitter] AND "LOC127814297"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 667155	NM_002700.3(POU4F3):c.295C>T (p.His99Tyr)	LOC127814297, POU4F3 (H99Y)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 15 +2 more	GConflicting classifications of pathogenicity
Select item 1712312	NM_002700.3(POU4F3):c.604G>A (p.Gly202Arg)	LOC127814297, POU4F3 (G202R)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 15	GUncertain significance