List of variants in gene combination LOC107982234, WT1 reported as uncertain significance for Meacham syndrome

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 29

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HGVS	dbSNP
NM_024426.6(WT1):c.-102C>A	rs886048240
NM_024426.6(WT1):c.-106C>T	rs867975105
NM_024426.6(WT1):c.-110C>T	rs886048241
NM_024426.6(WT1):c.-114T>A	rs886048242
NM_024426.6(WT1):c.-135G>A	rs886048243
NM_024426.6(WT1):c.-140C>T	rs886048244
NM_024426.6(WT1):c.-31G>T	rs886048234
NM_024426.6(WT1):c.-76T>C	rs886048235
NM_024426.6(WT1):c.-82A>C	rs886048236
NM_024426.6(WT1):c.-86T>C	rs886048237
NM_024426.6(WT1):c.-87C>T
NM_024426.6(WT1):c.-90T>C	rs886048238
NM_024426.6(WT1):c.-94G>C	rs886048239
NM_024426.6(WT1):c.124G>A (p.Gly42Ser)	rs762288656
NM_024426.6(WT1):c.136G>T (p.Ala46Ser)	rs886048233
NM_024426.6(WT1):c.162C>G (p.Ser54Arg)	rs776954184
NM_024426.6(WT1):c.174C>G (p.Leu58=)	rs886048232
NM_024426.6(WT1):c.193G>A (p.Gly65Arg)	rs374404615
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)
NM_024426.6(WT1):c.313G>T (p.Ala105Ser)
NM_024426.6(WT1):c.314C>G (p.Ala105Gly)	rs948061247
NM_024426.6(WT1):c.347C>T (p.Pro116Leu)	rs886048229
NM_024426.6(WT1):c.381C>G (p.Pro127=)	rs771681406
NM_024426.6(WT1):c.390A>G (p.Pro130=)	rs886048228
NM_024426.6(WT1):c.402G>A (p.Pro134=)
NM_024426.6(WT1):c.620T>G (p.Leu207Arg)
NM_024426.6(WT1):c.83G>A (p.Gly28Glu)	rs751641518

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