List of variants reported as uncertain significance for Proteinuria by Blueprint Genetics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_014625.4(NPHS2):c.686G>A (p.Arg229Gln)	rs61747728	0.02796
NM_004646.4(NPHS1):c.1802G>C (p.Gly601Ala)	rs114615449	0.00041
NM_004646.4(NPHS1):c.1610C>T (p.Thr537Met)	rs368913905	0.00027
NM_004646.4(NPHS1):c.2873G>A (p.Gly958Glu)	rs730880175	0.00004
NM_004646.4(NPHS1):c.1297C>T (p.Leu433Phe)	rs730880173	0.00001
NM_014625.4(NPHS2):c.817G>T (p.Gly273Trp)	rs201408880	0.00001
NM_022489.4(INF2):c.149A>C (p.Tyr50Ser)	rs730880113
NM_024426.6(WT1):c.764T>A (p.Met255Lys)	rs377573993

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