List of variants in gene COL4A4 reported as likely benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000092.5(COL4A4):c.948T>C (p.Tyr316=)	rs34509421	0.02777
NM_000092.5(COL4A4):c.2165-15T>G	rs60344965	0.02703
NM_000092.5(COL4A4):c.2276C>T (p.Pro759Leu)	rs36121515	0.02697
NM_000092.5(COL4A4):c.2899A>G (p.Ile967Val)	rs80243096	0.01747
NM_000092.5(COL4A4):c.3818-45T>A	rs55886181	0.01195
NM_000092.5(COL4A4):c.2717-5A>T	rs1800519	0.01182
NM_000092.5(COL4A4):c.666G>A (p.Pro222=)	rs111945121	0.00676
NM_000092.5(COL4A4):c.2907A>C (p.Ser969=)	rs116354015	0.00506
NM_000092.5(COL4A4):c.1833T>C (p.Gly611=)	rs145806603	0.00479
NM_000092.5(COL4A4):c.2630G>A (p.Arg877Gln)	rs150979437	0.00274
NM_000092.5(COL4A4):c.4152G>A (p.Ala1384=)	rs75398993	0.00245
NM_000092.5(COL4A4):c.4217-15T>C	rs200926310	0.00228
NM_000092.5(COL4A4):c.195T>C (p.Gly65=)	rs201278620	0.00082
NM_000092.5(COL4A4):c.1205-9A>G	rs370706928	0.00043
NM_000092.5(COL4A4):c.4349T>C (p.Ile1450Thr)	rs72969704	0.00038
NM_000092.5(COL4A4):c.3108T>C (p.Gly1036=)	rs201962241	0.00030
NM_000092.5(COL4A4):c.4334-3del	rs780415519

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