List of variants in gene combination COL4A3, MFF-DT reported as likely pathogenic for Benign familial hematuria

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.2083G>A (p.Gly695Arg)	rs200287952	0.00016
NM_000091.5(COL4A3):c.898G>A (p.Gly300Arg)	rs772708743	0.00002
NM_000091.5(COL4A3):c.1669G>A (p.Gly557Arg)	rs1457269547	0.00001
NM_000091.5(COL4A3):c.2498G>A (p.Gly833Asp)	rs779489401
NM_000091.5(COL4A3):c.3044G>A (p.Gly1015Glu)	rs121912826
NM_000091.5(COL4A3):c.3257G>A (p.Gly1086Glu)	rs1574813350
NM_000091.5(COL4A3):c.647G>T (p.Gly216Val)	rs2069899081

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