"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 523324	NM_000092.5(COL4A4):c.4394G>A (p.Gly1465Asp)	COL4A4 (G1465D)	Single nucleotide variant (missense variant)	Hypertensive disorder +8 more	GConflicting classifications of pathogenicity
Select item 255039	NM_000092.5(COL4A4):c.4217-15T>C	COL4A4	Single nucleotide variant (intron variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 374041	NM_000092.5(COL4A4):c.3055G>C (p.Glu1019Gln)	COL4A4 (E1019Q)	Single nucleotide variant (missense variant)	Hypertensive disorder +3 more	GUncertain significance
Select item 17406	NM_000092.5(COL4A4):c.2690G>A (p.Gly897Glu)	COL4A4 (G897E)	Single nucleotide variant (missense variant)	Benign familial hematuria +2 more	GPathogenic/Likely pathogenic
Select item 242442	NM_000092.5(COL4A4):c.2320G>C (p.Gly774Arg)	COL4A4 (G774R)	Single nucleotide variant (missense variant)	Hematuria +8 more	GConflicting classifications of pathogenicity
Select item 931925	NM_000092.5(COL4A4):c.1163G>T (p.Gly388Val)	COL4A4 (G388V)	Single nucleotide variant (missense variant)	Benign familial hematuria	GUncertain significance
Select item 931145	NM_000092.5(COL4A4):c.736-4del	COL4A4	Deletion (intron variant)	COL4A4-related disorder +2 more	GConflicting classifications of pathogenicity

ClinVar