ClinVar (all) for Orgtrack (Select 505876) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 252378	NM_194248.3(OTOF):c.1111G>C (p.Gly371Arg)	OTOF (G371R)	Single nucleotide variant (missense variant)	Hearing loss, autosomal recessive	GPathogenic
Select item 212012	NM_030665.4(RAI1):c.5254G>A (p.Gly1752Arg)	RAI1 (G1752R)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity