ClinVar (all) for Orgtrack (Select 508393) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1703255	NM_003742.4(ABCB11):c.617_619del (p.Ile206del)	ABCB11	Deletion (inframe_deletion)	Progressive familial intrahepatic cholestasis type 2	GLikely pathogenic
Select item 1345043	NM_001009944.3(PKD1):c.458C>A (p.Ala153Asp)	PKD1	Single nucleotide variant (missense variant)	Polycystic kidney disease, adult type	GLikely pathogenic