List of variants reported as uncertain significance for Dent disease type 1 by MVZ Medizinische Genetik Mainz

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001127898.4(CLCN5):c.1975C>T (p.Arg659Trp)	rs782594764	0.00001
NM_001127898.4(CLCN5):c.1191A>G (p.Ile397Met)	rs2519433878
NM_001127898.4(CLCN5):c.2129T>G (p.Leu710Arg)
NM_001127898.4(CLCN5):c.850_851delinsAA (p.Leu284Lys)
NM_001127898.4(CLCN5):c.950C>A (p.Ala317Glu)	rs2519431611

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