C4539881[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 431430	NM_001378457.1(DMXL2):c.7250G>A (p.Arg2417His)	DMXL2 (R2417H +4 more)	Single nucleotide variant (missense variant +1 more)	Hearing loss, autosomal dominant 71 +1 more	GConflicting classifications of pathogenicity
Select item 1065611	NM_001378457.1(DMXL2):c.918G>T (p.Gln306His)	DMXL2 (Q306H)	Single nucleotide variant (missense variant +1 more)	Hearing loss, autosomal dominant 71	GPathogenic