ClinVar Miner

List of variants in gene WT1 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_024426.6(WT1):c.*1049del rs568803808
NM_024426.6(WT1):c.*267G>C rs5030317
NM_024426.6(WT1):c.*602A>G rs5030320
NM_024426.6(WT1):c.*978dup rs5030326
NM_024426.6(WT1):c.1017-9T>C rs368486676
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.1161A>G (p.Ala387=) rs141834493
NM_024426.6(WT1):c.1265-32C>A rs2234593
NM_024426.6(WT1):c.1265-52G>T rs869312745
NM_024426.6(WT1):c.1448-10G>A rs185744719
NM_024426.6(WT1):c.696C>T (p.Ser232=) rs9332974

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