ClinVar (all) for Orgtrack (Select 506193) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 430716	NM_033380.3(COL4A5):c.1960G>T (p.Asp654Tyr)	COL4A5 (D654Y)	Single nucleotide variant (missense variant)	Familial hematuria	GLikely pathogenic
Select item 430574	NM_005560.6(LAMA5):c.3728C>T (p.Pro1243Leu)	LAMA5 (P1243L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance