List of variants in gene combination COL4A3, MFF-DT 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.112C>G (p.Gln38Glu)	rs201607115	0.00132
NM_000091.5(COL4A3):c.4295G>A (p.Arg1432His)	rs200509072	0.00074
NM_000091.5(COL4A3):c.3829G>A (p.Gly1277Ser)	rs190598500	0.00032
NM_000091.5(COL4A3):c.3945A>G (p.Pro1315=)	rs189574905	0.00021
NM_000091.5(COL4A3):c.3094T>C (p.Leu1032=)	rs372423505	0.00012
NM_000091.5(COL4A3):c.4449C>T (p.His1483=)	rs140672401	0.00012
NM_000091.5(COL4A3):c.1790C>T (p.Pro597Leu)	rs781163705	0.00011
NM_000091.5(COL4A3):c.3476G>A (p.Arg1159His)	rs145948549	0.00009
NM_000091.5(COL4A3):c.3755C>T (p.Ala1252Val)	rs761179248	0.00009
NM_000091.5(COL4A3):c.4482G>A (p.Leu1494=)	rs181952966	0.00005
NM_000091.5(COL4A3):c.2133A>G (p.Gln711=)	rs527383673	0.00004
NM_000091.5(COL4A3):c.516C>T (p.Asp172=)	rs759455097	0.00003
NM_000091.5(COL4A3):c.3690C>T (p.Pro1230=)	rs375442737	0.00001
NM_000091.5(COL4A3):c.3825C>T (p.His1275=)	rs143380907

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