List of variants in gene combination COL4A3, LOC129935730 reported as likely benign for autosomal dominant Alport syndrome

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.21C>A (p.Pro7=)	rs530353117	0.00045
NM_000091.5(COL4A3):c.-10C>T	rs781380101	0.00039
NM_000091.5(COL4A3):c.63G>A (p.Leu21=)	rs1036829250	0.00008
NM_000091.5(COL4A3):c.45G>A (p.Pro15=)	rs542100614	0.00001
NM_000091.5(COL4A3):c.43_54del (p.Pro15_Leu18del)	rs570469692

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