ClinVar (all) for Orgtrack (Select 507049) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 634651	NM_000092.4(COL4A4):c.3861delinsCTC (p.Arg1288fs)	COL4A4	Indel	not provided	GLikely pathogenic
Select item 634650	NM_000092.5(COL4A4):c.4708G>A (p.Glu1570Lys)	COL4A4 (E1570K)	Single nucleotide variant (missense variant)	Autosomal recessive Alport syndrome +3 more	GUncertain significance