ClinVar Miner

List of variants in gene WT1 reported as likely benign for not provided

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.1265-249C>T rs113403661 0.01542
NM_024426.6(WT1):c.1114-160G>A rs73473740 0.01502
NM_024426.6(WT1):c.888-98G>A rs5030196 0.01071
NM_024426.6(WT1):c.785-172A>C rs144615463 0.01005
NM_024426.6(WT1):c.1016+81C>T rs5030208 0.00829
NM_024426.6(WT1):c.1265-173C>T rs149529057 0.00822
NM_024426.6(WT1):c.1355-87G>A rs5030290 0.00796
NM_024426.6(WT1):c.1265-141T>G rs5030288 0.00768
NM_024426.6(WT1):c.662-211G>C rs5030164 0.00737
NM_024426.6(WT1):c.887+229G>A rs5030173 0.00617
NM_024426.6(WT1):c.1114-9T>C rs5030274 0.00465
NM_024426.6(WT1):c.*16G>T rs2234594 0.00421
NM_024426.6(WT1):c.785-160T>C rs186598490 0.00116
NM_024426.6(WT1):c.1131T>C (p.Pro377=) rs151034312 0.00047
NM_024426.6(WT1):c.662-6C>A rs372418954 0.00034
NM_024426.6(WT1):c.760C>T (p.Pro254Ser) rs2234584 0.00022
NM_024426.6(WT1):c.1146T>A (p.Thr382=) rs371168589 0.00006
NM_024426.6(WT1):c.1404C>T (p.Ser468=) rs374799820 0.00006
NM_024426.6(WT1):c.1568G>A (p.Ter523=) rs148856160 0.00001
NM_024426.6(WT1):c.1265-218del rs111384963
NM_024426.6(WT1):c.1448-10G>T rs185744719
NM_024426.6(WT1):c.662-80del rs34924443
NM_024426.6(WT1):c.785-14G>C rs375514482
NR_023920.1(WT1-AS):n.1514C>T
NR_023920.2(WT1-AS):n.791T>C

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