ClinVar Miner

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

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.-110C>T rs886048241 0.00048
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 0.00018
NM_024426.6(WT1):c.343C>T (p.Pro115Ser) rs916583720 0.00011
NM_024426.6(WT1):c.381C>G (p.Pro127=) rs771681406 0.00009
NM_024426.6(WT1):c.314C>G (p.Ala105Gly) rs948061247 0.00008
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.29C>T (p.Ala10Val) rs997104313 0.00006
NM_024426.6(WT1):c.402G>A (p.Pro134=) rs777527675 0.00003
NM_024426.6(WT1):c.591G>T (p.Gln197His) rs767850217 0.00003
NM_024426.6(WT1):c.661+6T>C rs557166021 0.00003
NM_024426.6(WT1):c.151del (p.Ala51fs) rs776155094 0.00002
NM_024426.6(WT1):c.218A>T (p.Gln73Leu) rs1036899554 0.00002
NM_024426.6(WT1):c.223G>A (p.Gly75Ser) rs528076586 0.00002
NM_024426.6(WT1):c.248C>T (p.Ala83Val) rs1278102757 0.00002
NM_024426.6(WT1):c.386C>A (p.Pro129Gln) rs745435848 0.00002
NM_024426.6(WT1):c.658C>A (p.Gln220Lys) rs373935628 0.00002
NM_024426.6(WT1):c.149C>A (p.Ala50Asp) rs967658170 0.00001
NM_024426.6(WT1):c.172C>G (p.Leu58Val) rs1412425868 0.00001
NM_024426.6(WT1):c.174C>G (p.Leu58=) rs886048232 0.00001
NM_024426.6(WT1):c.211C>A (p.Pro71Thr) rs1392405207 0.00001
NM_024426.6(WT1):c.26C>T (p.Pro9Leu) rs948132360 0.00001
NM_024426.6(WT1):c.34A>C (p.Thr12Pro) rs764111950 0.00001
NM_024426.6(WT1):c.392C>G (p.Pro131Arg) rs1443423967 0.00001
NM_024426.6(WT1):c.412C>T (p.Pro138Ser) rs544477985 0.00001
NM_024426.6(WT1):c.439C>G (p.Gln147Glu) rs953087575 0.00001
NM_024426.6(WT1):c.459C>T (p.Gly153=) rs1309250331 0.00001
NM_024426.6(WT1):c.491C>T (p.Ala164Val) rs1853443839 0.00001
NM_024426.6(WT1):c.542G>C (p.Arg181Pro) rs1853441270 0.00001
NM_024426.6(WT1):c.583T>G (p.Ser195Ala) rs975173030 0.00001
NM_024426.6(WT1):c.620T>G (p.Leu207Arg) rs1258754686 0.00001
NM_024426.6(WT1):c.628T>G (p.Cys210Gly) rs776426005 0.00001
NM_024426.6(WT1):c.641A>C (p.Gln214Pro) rs771024882 0.00001
NM_024426.6(WT1):c.646G>A (p.Ala216Thr) rs778069787 0.00001
NM_024426.6(WT1):c.77G>A (p.Gly26Glu) rs1484558172 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.10C>G (p.Leu4Val)
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.163G>A (p.Ala55Thr) rs1853472865
NM_024426.6(WT1):c.16_17delinsGG (p.Leu6Gly) rs2494490498
NM_024426.6(WT1):c.203G>A (p.Gly68Glu) rs1170323988
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.28_29delinsTA (p.Ala10Tyr) rs1554946803
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.347C>T (p.Pro116Leu) rs886048229
NM_024426.6(WT1):c.351C>T (p.Gly117=) rs1473590912
NM_024426.6(WT1):c.376G>A (p.Gly126Ser) rs1853454814
NM_024426.6(WT1):c.386C>T (p.Pro129Leu) rs745435848
NM_024426.6(WT1):c.390A>G (p.Pro130=) rs886048228
NM_024426.6(WT1):c.410C>G (p.Pro137Arg)
NM_024426.6(WT1):c.411GCC[5] (p.Pro141dup) rs760304811
NM_024426.6(WT1):c.430_432del (p.Phe144del) rs1262223289
NM_024426.6(WT1):c.437A>G (p.Lys146Arg)
NM_024426.6(WT1):c.443A>G (p.Glu148Gly)
NM_024426.6(WT1):c.467C>T (p.Pro156Leu) rs1225927150
NM_024426.6(WT1):c.513C>T (p.Gly171=) rs536728682
NM_024426.6(WT1):c.530C>T (p.Ala177Val)
NM_024426.6(WT1):c.539G>A (p.Cys180Tyr) rs2133102350
NM_024426.6(WT1):c.544T>C (p.Tyr182His) rs2494477429
NM_024426.6(WT1):c.568C>G (p.Pro190Ala)
NM_024426.6(WT1):c.600G>A (p.Met200Ile) rs1060501257
NM_024426.6(WT1):c.617A>T (p.Tyr206Phe)
NM_024426.6(WT1):c.61C>T (p.His21Tyr)
NM_024426.6(WT1):c.653G>A (p.Arg218His) rs756414084
NM_024426.6(WT1):c.661+15G>T rs1362460137

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