ClinVar Miner

List of variants in gene WT1 reported as benign for Meacham syndrome

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_024426.6(WT1):c.*1049del rs568803808
NM_024426.6(WT1):c.*1098C>T rs5030327
NM_024426.6(WT1):c.*1132A>T rs5030328
NM_024426.6(WT1):c.*1209A>G rs5030329
NM_024426.6(WT1):c.*1239T>A rs534396876
NM_024426.6(WT1):c.*12C>T
NM_024426.6(WT1):c.*16G>T rs2234594
NM_024426.6(WT1):c.*224A>G rs5030316
NM_024426.6(WT1):c.*267G>C rs5030317
NM_024426.6(WT1):c.*345G>A rs5030318
NM_024426.6(WT1):c.*602A>G rs5030320
NM_024426.6(WT1):c.*820G>C rs1042347
NM_024426.6(WT1):c.*835A>G rs5030322
NM_024426.6(WT1):c.*864T>A rs5030323
NM_024426.6(WT1):c.*864T>G rs5030323
NM_024426.6(WT1):c.*88A>G rs5030315
NM_024426.6(WT1):c.*903G>A rs5030325
NM_024426.6(WT1):c.*978dup rs5030326
NM_024426.6(WT1):c.1017-9T>C rs368486676
NM_024426.6(WT1):c.1020C>T (p.His340=)
NM_024426.6(WT1):c.1074A>G (p.Gln358=) rs2234590
NM_024426.6(WT1):c.1114-9T>C rs5030274
NM_024426.6(WT1):c.1122A>G (p.Arg374=) rs16754
NM_024426.6(WT1):c.1124G>A (p.Arg375His) rs554416372
NM_024426.6(WT1):c.1131T>C (p.Pro377=) rs151034312
NM_024426.6(WT1):c.1154G>A (p.Arg385Gln) rs147241955
NM_024426.6(WT1):c.1182C>T (p.Arg394=) rs147939483
NM_024426.6(WT1):c.695G>C (p.Ser232Thr) rs761913397
NM_024426.6(WT1):c.696C>T (p.Ser232=) rs9332974
NM_024426.6(WT1):c.760C>T (p.Pro254Ser) rs2234584

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