List of variants in gene combination COL4A3, LOC129935730 reported as uncertain significance for 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.-13G>C	rs770803750	0.00217
NM_000091.5(COL4A3):c.-10C>T	rs781380101	0.00039
NM_000091.5(COL4A3):c.-26G>T	rs747049729	0.00019
NM_000091.5(COL4A3):c.63G>A (p.Leu21=)	rs1036829250	0.00008
NM_000091.5(COL4A3):c.11G>A (p.Arg4Gln)	rs921905047	0.00007
NM_000091.5(COL4A3):c.-16T>C	rs886055736	0.00002
NM_000091.5(COL4A3):c.36C>T (p.Leu12=)	rs1189095338
NM_000091.5(COL4A3):c.87+7G>T	rs1358691399

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