List of variants in gene combination COL4A3, MFF-DT reported as likely benign for Autosomal dominant Alport syndrome; Hematuria, benign familial, 2; Alport syndrome 3b, autosomal recessive

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.1483C>T (p.His495Tyr)	rs200510532	0.00110
NM_000091.5(COL4A3):c.2168C>T (p.Pro723Leu)	rs201198284	0.00021
NM_000091.5(COL4A3):c.1437C>T (p.Cys479=)	rs748691382	0.00003

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