ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
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Gene type:
ClinVar version:
Total variants: 114
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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.-90T>C rs886048238
NM_024426.6(WT1):c.-94G>C rs886048239
NM_024426.6(WT1):c.112G>C (p.Val38Leu)
NM_024426.6(WT1):c.116G>A (p.Arg39Gln)
NM_024426.6(WT1):c.121C>G (p.Pro41Ala)
NM_024426.6(WT1):c.121C>T (p.Pro41Ser) rs926668379
NM_024426.6(WT1):c.124G>A (p.Gly42Ser) rs762288656
NM_024426.6(WT1):c.133T>C (p.Trp45Arg) rs1186470250
NM_024426.6(WT1):c.136G>A (p.Ala46Thr)
NM_024426.6(WT1):c.136G>T (p.Ala46Ser) rs886048233
NM_024426.6(WT1):c.143T>C (p.Leu48Ser) rs1565002394
NM_024426.6(WT1):c.146G>T (p.Gly49Val) rs1475923286
NM_024426.6(WT1):c.151del (p.Ala51fs) rs776155094
NM_024426.6(WT1):c.162C>G (p.Ser54Arg) rs776954184
NM_024426.6(WT1):c.172C>G (p.Leu58Val) rs1412425868
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.193G>T (p.Gly65Trp)
NM_024426.6(WT1):c.196G>A (p.Ala66Thr)
NM_024426.6(WT1):c.200C>G (p.Ser67Cys) rs1327516147
NM_024426.6(WT1):c.200C>T (p.Ser67Phe) rs1327516147
NM_024426.6(WT1):c.203G>A (p.Gly68Glu) rs1170323988
NM_024426.6(WT1):c.205T>A (p.Ser69Thr) rs1565002158
NM_024426.6(WT1):c.218A>T (p.Gln73Leu) rs1036899554
NM_024426.6(WT1):c.223G>A (p.Gly75Ser)
NM_024426.6(WT1):c.232G>A (p.Val78Met)
NM_024426.6(WT1):c.247G>C (p.Ala83Pro) rs886048231
NM_024426.6(WT1):c.247G>T (p.Ala83Ser) rs886048231
NM_024426.6(WT1):c.248C>T (p.Ala83Val) rs1278102757
NM_024426.6(WT1):c.268T>C (p.Ser90Pro)
NM_024426.6(WT1):c.26C>G (p.Pro9Arg)
NM_024426.6(WT1):c.277_279GGC[3] (p.Gly96del) rs770519620
NM_024426.6(WT1):c.278G>A (p.Gly93Asp)
NM_024426.6(WT1):c.285C>T (p.Gly95=) rs886048230
NM_024426.6(WT1):c.286G>A (p.Gly96Ser) rs1060501254
NM_024426.6(WT1):c.28_29delinsAT (p.Ala10Ile) rs1554946803
NM_024426.6(WT1):c.28_29delinsTA (p.Ala10Tyr) rs1554946803
NM_024426.6(WT1):c.296T>C (p.Leu99Pro) rs1565001942
NM_024426.6(WT1):c.298C>A (p.Pro100Thr)
NM_024426.6(WT1):c.29C>A (p.Ala10Asp)
NM_024426.6(WT1):c.29C>T (p.Ala10Val)
NM_024426.6(WT1):c.300T>A (p.Pro100=) rs1255257323
NM_024426.6(WT1):c.307G>T (p.Gly103Cys) rs1348287926
NM_024426.6(WT1):c.314C>A (p.Ala105Glu)
NM_024426.6(WT1):c.314C>G (p.Ala105Gly) rs948061247
NM_024426.6(WT1):c.320G>T (p.Trp107Leu)
NM_024426.6(WT1):c.340G>A (p.Ala114Thr)
NM_024426.6(WT1):c.341C>A (p.Ala114Glu)
NM_024426.6(WT1):c.341C>T (p.Ala114Val) rs1311557029
NM_024426.6(WT1):c.343C>T (p.Pro115Ser) rs916583720
NM_024426.6(WT1):c.344C>A (p.Pro115His) rs1565001804
NM_024426.6(WT1):c.346C>A (p.Pro116Thr) rs1554946595
NM_024426.6(WT1):c.347C>T (p.Pro116Leu) rs886048229
NM_024426.6(WT1):c.34A>C (p.Thr12Pro) rs764111950
NM_024426.6(WT1):c.352G>A (p.Ala118Thr) rs1253163678
NM_024426.6(WT1):c.355T>C (p.Ser119Pro) rs1187111469
NM_024426.6(WT1):c.358G>A (p.Ala120Thr)
NM_024426.6(WT1):c.375C>T (p.Gly125=) rs776209354
NM_024426.6(WT1):c.379C>A (p.Pro127Thr) rs1554946578
NM_024426.6(WT1):c.380C>G (p.Pro127Arg)
NM_024426.6(WT1):c.381C>G (p.Pro127=) rs771681406
NM_024426.6(WT1):c.386C>A (p.Pro129Gln)
NM_024426.6(WT1):c.386C>T (p.Pro129Leu)
NM_024426.6(WT1):c.388C>T (p.Pro130Ser) rs1554946573
NM_024426.6(WT1):c.390A>G (p.Pro130=) rs886048228
NM_024426.6(WT1):c.391C>T (p.Pro131Ser)
NM_024426.6(WT1):c.397C>A (p.Pro133Thr) rs1202603651
NM_024426.6(WT1):c.404C>T (p.Pro135Leu) rs769642496
NM_024426.6(WT1):c.411_413GCC[5] (p.Pro141dup) rs760304811
NM_024426.6(WT1):c.416C>G (p.Pro139Arg) rs878855085
NM_024426.6(WT1):c.419C>T (p.Pro140Leu)
NM_024426.6(WT1):c.421C>T (p.Pro141Ser) rs750548251
NM_024426.6(WT1):c.425A>C (p.His142Pro) rs1565001515
NM_024426.6(WT1):c.439C>G (p.Gln147Glu) rs953087575
NM_024426.6(WT1):c.440A>G (p.Gln147Arg)
NM_024426.6(WT1):c.445C>T (p.Pro149Ser) rs1554946517
NM_024426.6(WT1):c.450C>A (p.Ser150Arg) rs1213710686
NM_024426.6(WT1):c.45G>A (p.Pro15=)
NM_024426.6(WT1):c.471C>A (p.His157Gln)
NM_024426.6(WT1):c.475G>A (p.Glu159Lys) rs768165877
NM_024426.6(WT1):c.480G>C (p.Gln160His)
NM_024426.6(WT1):c.512G>T (p.Gly171Val) rs1554946480
NM_024426.6(WT1):c.52G>C (p.Ala18Pro)
NM_024426.6(WT1):c.541C>A (p.Arg181Ser) rs1565001278
NM_024426.6(WT1):c.548G>A (p.Gly183Glu) rs1060501256
NM_024426.6(WT1):c.562C>T (p.Pro188Ser) rs1565001232
NM_024426.6(WT1):c.584C>G (p.Ser195Cys) rs778194188
NM_024426.6(WT1):c.586G>A (p.Gly196Ser)
NM_024426.6(WT1):c.587G>A (p.Gly196Asp) rs753112302
NM_024426.6(WT1):c.591G>T (p.Gln197His)
NM_024426.6(WT1):c.600G>A (p.Met200Ile) rs1060501257
NM_024426.6(WT1):c.609C>G (p.Asn203Lys) rs2234583
NM_024426.6(WT1):c.610G>T (p.Ala204Ser)
NM_024426.6(WT1):c.615C>G (p.Pro205=) rs769467940
NM_024426.6(WT1):c.641A>C (p.Gln214Pro)
NM_024426.6(WT1):c.649A>G (p.Ile217Val) rs1384974578
NM_024426.6(WT1):c.653G>T (p.Arg218Leu) rs756414084
NM_024426.6(WT1):c.658C>A (p.Gln220Lys)
NM_024426.6(WT1):c.659A>G (p.Gln220Arg) rs1554946409
NM_024426.6(WT1):c.661+6T>C rs557166021
NM_024426.6(WT1):c.70C>T (p.Arg24Cys) rs878855086
NM_024426.6(WT1):c.77G>A (p.Gly26Glu) rs1484558172
NM_024426.6(WT1):c.83G>A (p.Gly28Glu) rs751641518
NM_024426.6(WT1):c.86G>A (p.Cys29Tyr) rs992227366

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