List of variants reported as uncertain significance for Finnish congenital nephrotic syndrome by Revvity Omics, Revvity

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004646.4(NPHS1):c.2405G>A (p.Arg802Gln)	rs114203578	0.00028
NM_004646.4(NPHS1):c.1289A>G (p.Lys430Arg)	rs368523939	0.00003
NM_004646.4(NPHS1):c.1196T>C (p.Met399Thr)	rs781420585	0.00001
NM_004646.4(NPHS1):c.1744A>G (p.Lys582Glu)	rs1973129439	0.00001
NM_004646.4(NPHS1):c.1240A>G (p.Thr414Ala)	rs1973174583
NM_004646.4(NPHS1):c.515_517del (p.Thr172del)	rs386833947

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