List of variants reported as uncertain significance for Finnish congenital nephrotic syndrome by Illumina Laboratory Services, Illumina

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004646.4(NPHS1):c.1440+11C>T	rs750251097	0.00001
NM_004646.4(NPHS1):c.*488T>C	rs886054346
NM_004646.4(NPHS1):c.2159A>C (p.His720Pro)	rs760911714
NM_004646.4(NPHS1):c.726C>T (p.Pro242=)	rs886054352

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