ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported as likely benign by GeneDx

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.662-2310C>T rs3847590 0.01761
NM_024426.6(WT1):c.661+161G>T rs5030139 0.01255
NM_024426.6(WT1):c.661+58C>T rs5030138 0.00604
NM_024426.6(WT1):c.662-2299A>C rs192410368 0.00601
NM_024426.6(WT1):c.309C>A (p.Gly103=) rs547333427 0.00197
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661 0.00188
NM_024426.6(WT1):c.662-1873_662-1868dup rs1554945689 0.00091
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135 0.00036
NM_024426.6(WT1):c.193G>A (p.Gly65Arg) rs374404615 0.00019
NM_024426.6(WT1):c.381C>G (p.Pro127=) rs771681406 0.00009
NM_024426.6(WT1):c.421C>T (p.Pro141Ser) rs750548251 0.00009
NM_024426.6(WT1):c.513C>A (p.Gly171=) rs536728682 0.00004
NM_024426.6(WT1):c.662-1831CT[8] rs370524588
NM_024426.6(WT1):c.662-1836_662-1835dup rs367920789
NR_023920.2(WT1-AS):n.323C>A rs2234579

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