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

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Total variants: 53

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HGVS	dbSNP
NM_004646.3(NPHS1):c.*1020C>T	rs564256430
NM_004646.3(NPHS1):c.*1021G>A	rs536792618
NM_004646.3(NPHS1):c.*1040C>T	rs181405524
NM_004646.3(NPHS1):c.*250G>A	rs117894015
NM_004646.3(NPHS1):c.*488T>C	rs886054346
NM_004646.3(NPHS1):c.*529C>T	rs148755697
NM_004646.3(NPHS1):c.*609G>A	rs144206206
NM_004646.3(NPHS1):c.*706A>G	rs80296922
NM_004646.3(NPHS1):c.*759A>T	rs886054345
NM_004646.3(NPHS1):c.*82G>T	rs569295487
NM_004646.3(NPHS1):c.*958G>T	rs886054344
NM_004646.3(NPHS1):c.-31C>T	rs376050812
NM_004646.3(NPHS1):c.-57G>T	rs140404523
NM_004646.3(NPHS1):c.-61G>A	rs75799457
NM_004646.3(NPHS1):c.1110T>C (p.Val370=)	rs116459838
NM_004646.3(NPHS1):c.115G>A (p.Glu39Lys)	rs375670819
NM_004646.3(NPHS1):c.1170+8G>A	rs140808195
NM_004646.3(NPHS1):c.1440+11C>T	rs750251097
NM_004646.3(NPHS1):c.1440+2T>C	rs1568455470
NM_004646.3(NPHS1):c.151C>T (p.Leu51=)	rs114385015
NM_004646.3(NPHS1):c.1598T>C (p.Leu533Pro)	rs886054351
NM_004646.3(NPHS1):c.1638T>G (p.Thr546=)	rs115444936
NM_004646.3(NPHS1):c.1758-11C>G	rs145554982
NM_004646.3(NPHS1):c.1799A>G (p.Lys600Arg)	rs566516658
NM_004646.3(NPHS1):c.1802G>C (p.Gly601Ala)	rs114615449
NM_004646.3(NPHS1):c.1861G>A (p.Val621Met)	rs886054350
NM_004646.3(NPHS1):c.1926A>G (p.Val642=)	rs114728208
NM_004646.3(NPHS1):c.1930+10C>T	rs76131336
NM_004646.3(NPHS1):c.2072C>A (p.Ala691Glu)	rs886054349
NM_004646.3(NPHS1):c.2469G>A (p.Ala823=)	rs371646734
NM_004646.3(NPHS1):c.2654A>T (p.Gln885Leu)	rs886054348
NM_004646.3(NPHS1):c.2686C>G (p.Gln896Glu)	rs771594710
NM_004646.3(NPHS1):c.2916G>T (p.Arg972Ser)	rs374762054
NM_004646.3(NPHS1):c.2961T>C (p.Tyr987=)	rs201263480
NM_004646.3(NPHS1):c.3166+14C>A	rs886054347
NM_004646.3(NPHS1):c.319G>A (p.Ala107Thr)	rs386833933
NM_004646.3(NPHS1):c.3206T>C (p.Leu1069Pro)	rs756273676
NM_004646.3(NPHS1):c.3311+14T>C	rs375587420
NM_004646.3(NPHS1):c.3364G>C (p.Glu1122Gln)	rs548792892
NM_004646.3(NPHS1):c.3388-14C>T	rs371907999
NM_004646.3(NPHS1):c.3419G>A (p.Arg1140His)	rs369787477
NM_004646.3(NPHS1):c.3555_3574del (p.Ser1186fs)	rs767832658
NM_004646.3(NPHS1):c.397+15C>T	rs78237760
NM_004646.3(NPHS1):c.427G>C (p.Glu143Gln)	rs540253444
NM_004646.3(NPHS1):c.428A>T (p.Glu143Val)	rs781117481
NM_004646.3(NPHS1):c.485C>G (p.Ser162Cys)	rs376172729
NM_004646.3(NPHS1):c.505C>A (p.Pro169Thr)	rs886054353
NM_004646.3(NPHS1):c.597G>A (p.Glu199=)	rs61731102
NM_004646.3(NPHS1):c.726C>T (p.Pro242=)	rs886054352
NM_004646.3(NPHS1):c.733A>C (p.Ile245Leu)	rs370046047
NM_004646.3(NPHS1):c.772G>T (p.Gly258Ter)	rs1568456335
NM_004646.3(NPHS1):c.895C>T (p.Arg299Cys)	rs753476209
NM_004646.3(NPHS1):c.916G>A (p.Val306Met)	rs769719915

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