List of variants in gene combination LOC107982234, WT1 reported as uncertain significance for Nephrotic syndrome, type 4

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.309C>A (p.Gly103=)	rs547333427	0.00197
NM_024426.6(WT1):c.-110C>T	rs886048241	0.00048
NM_024426.6(WT1):c.375C>T (p.Gly125=)	rs776209354	0.00039
NM_024426.6(WT1):c.-76T>C	rs886048235	0.00032
NM_024426.6(WT1):c.-106C>T	rs867975105	0.00021
NM_024426.6(WT1):c.124G>A (p.Gly42Ser)	rs762288656	0.00019
NM_024426.6(WT1):c.193G>A (p.Gly65Arg)	rs374404615	0.00019
NM_024426.6(WT1):c.381C>G (p.Pro127=)	rs771681406	0.00009
NM_024426.6(WT1):c.-140C>T	rs886048244	0.00006
NM_024426.6(WT1):c.162C>G (p.Ser54Arg)	rs776954184	0.00006
NM_024426.6(WT1):c.587G>A (p.Gly196Asp)	rs753112302	0.00002
NM_024426.6(WT1):c.620T>G (p.Leu207Arg)	rs1258754686	0.00001
NM_024426.6(WT1):c.83G>A (p.Gly28Glu)	rs751641518	0.00001
NM_024426.6(WT1):c.-102C>A	rs886048240
NM_024426.6(WT1):c.-114T>A	rs886048242
NM_024426.6(WT1):c.-135G>A	rs886048243
NM_024426.6(WT1):c.-31G>T	rs886048234
NM_024426.6(WT1):c.-82A>C	rs886048236
NM_024426.6(WT1):c.-86T>C	rs886048237
NM_024426.6(WT1):c.-87C>T	rs1395440150
NM_024426.6(WT1):c.-90T>C	rs886048238
NM_024426.6(WT1):c.-94G>C	rs886048239
NM_024426.6(WT1):c.136G>T (p.Ala46Ser)	rs886048233
NM_024426.6(WT1):c.174C>G (p.Leu58=)	rs886048232
NM_024426.6(WT1):c.247G>T (p.Ala83Ser)	rs886048231
NM_024426.6(WT1):c.285C>T (p.Gly95=)	rs886048230
NM_024426.6(WT1):c.298C>G (p.Pro100Ala)	rs567200038
NM_024426.6(WT1):c.313G>T (p.Ala105Ser)	rs1236417259
NM_024426.6(WT1):c.341C>T (p.Ala114Val)	rs1311557029
NM_024426.6(WT1):c.347C>T (p.Pro116Leu)	rs886048229
NM_024426.6(WT1):c.390A>G (p.Pro130=)	rs886048228
NM_024426.6(WT1):c.402G>A (p.Pro134=)	rs777527675
NM_024426.6(WT1):c.512G>T (p.Gly171Val)	rs1554946480

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