ClinVar Miner

List of variants reported as uncertain significance for Autosomal dominant Alport syndrome by 3billion

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.765G>A (p.Thr255=)	rs869025328	0.00001
NM_000091.5(COL4A3):c.1621G>T (p.Gly541Cys)
NM_000091.5(COL4A3):c.3026G>A (p.Gly1009Glu)

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