ClinVar Miner

List of variants reported as benign for Meacham syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.*602A>G rs5030320 0.45163
NM_024426.6(WT1):c.*267G>C rs5030317 0.44381
NM_024426.6(WT1):c.1448-49T>C rs1799937 0.34839
NM_024426.6(WT1):c.213G>T (p.Pro71=) rs2234582 0.31689
NM_024426.6(WT1):c.887+16G>A rs1799933 0.26810
NM_024426.6(WT1):c.1122A>G (p.Arg374=) rs16754 0.16617
NM_024426.6(WT1):c.345C>T (p.Pro115=) rs1799925 0.15374
NM_024426.6(WT1):c.*88A>G rs5030315 0.14706
NM_024426.6(WT1):c.*224A>G rs5030316 0.13669
NM_024426.6(WT1):c.609C>T (p.Asn203=) rs2234583 0.13287
NM_024426.6(WT1):c.1265-32C>A rs2234593 0.12726
NM_024426.6(WT1):c.1074A>G (p.Gln358=) rs2234590 0.04693
NM_024426.6(WT1):c.*820G>C rs1042347 0.03223
NM_024426.6(WT1):c.*1132A>T rs5030328 0.02340
NM_024426.6(WT1):c.*835A>G rs5030322 0.02303
NM_024426.6(WT1):c.662-1928_662-1927del rs71873106 0.02282
NM_024426.6(WT1):c.*1209A>G rs5030329 0.00900
NM_024426.6(WT1):c.*1098C>T rs5030327 0.00867
NM_024426.6(WT1):c.785-20G>T rs5030168 0.00663
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.*903G>A rs5030325 0.00370
NM_024426.6(WT1):c.181C>A (p.Arg61=) rs2234581 0.00270
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661 0.00188
NM_024426.6(WT1):c.1131T>C (p.Pro377=) rs151034312 0.00047
NM_024426.6(WT1):c.375C>T (p.Gly125=) rs776209354 0.00039
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135 0.00036
NM_024426.6(WT1):c.*12C>T rs77462662 0.00034
NM_024426.6(WT1):c.1182C>T (p.Arg394=) rs147939483 0.00027
NM_024426.6(WT1):c.760C>T (p.Pro254Ser) rs2234584 0.00022
NM_024426.6(WT1):c.1017-9T>C rs368486676 0.00007
NM_024426.6(WT1):c.1020C>T (p.His340=) rs375114529 0.00007
NM_024426.6(WT1):c.696C>T (p.Ser232=) rs9332974 0.00006
NM_024426.6(WT1):c.513C>A (p.Gly171=) rs536728682 0.00004
NM_024426.6(WT1):c.1124G>A (p.Arg375His) rs554416372 0.00003
NM_024426.6(WT1):c.1154G>A (p.Arg385Gln) rs147241955 0.00003
NM_024426.6(WT1):c.*1049del rs568803808
NM_024426.6(WT1):c.*1239T>A rs534396876
NM_024426.6(WT1):c.*345G>A rs5030318
NM_024426.6(WT1):c.*864T>A rs5030323
NM_024426.6(WT1):c.*864T>G rs5030323
NM_024426.6(WT1):c.*978dup rs5030326
NM_024426.6(WT1):c.695G>C (p.Ser232Thr) rs761913397

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