List of variants in gene COL4A4 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000092.5(COL4A4):c.50A>G (p.Lys17Arg)	rs114969026	0.00341
NM_000092.5(COL4A4):c.4217-15T>C	rs200926310	0.00228
NM_000092.5(COL4A4):c.2241C>T (p.Pro747=)	rs374510402	0.00048
NM_000092.5(COL4A4):c.4349T>C (p.Ile1450Thr)	rs72969704	0.00038
NM_000092.5(COL4A4):c.3666T>C (p.Pro1222=)	rs372838090	0.00029
NM_000092.5(COL4A4):c.2430C>G (p.Gly810=)	rs769363556	0.00015
NM_000092.5(COL4A4):c.3995C>T (p.Pro1332Leu)	rs200860702	0.00009
NM_000092.5(COL4A4):c.928C>T (p.Arg310Trp)	rs200817090	0.00005
NM_000092.5(COL4A4):c.888G>A (p.Gly296=)	rs746239973	0.00003
NM_000092.5(COL4A4):c.2319G>A (p.Arg773=)	rs200920187
NM_000092.5(COL4A4):c.2647C>A (p.Pro883Thr)	rs200761108
NM_000092.5(COL4A4):c.297T>A (p.Pro99=)	rs1576662029
NM_000092.5(COL4A4):c.4334-3del	rs780415519
NM_000092.5(COL4A4):c.4760C>G (p.Pro1587Arg)	rs190148408

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