"AiLife Diagnostics, AiLife Diagnostics"[submitter] AND "OXTR"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 804667	NM_033337.3(CAV3):c.266G>A (p.Gly89Asp)	CAV3, OXTR (G89D)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 180798	NM_033337.3(CAV3):c.277G>T (p.Ala93Ser)	CAV3, OXTR (A93S)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 191444	NM_033337.3(CAV3):c.294C>A (p.Cys98Ter)	CAV3, OXTR (C98*)	Single nucleotide variant (nonsense)	not provided +1 more	GConflicting classifications of pathogenicity

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ClinVar