ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported as likely benign for Denys-Drash syndrome

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661
NM_024426.6(WT1):c.150C>T (p.Ala50=) rs1554946724
NM_024426.6(WT1):c.181C>A (p.Arg61=) rs2234581
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135
NM_024426.6(WT1):c.309C>A (p.Gly103=) rs547333427
NM_024426.6(WT1):c.315G>A (p.Ala105=) rs1554946607
NM_024426.6(WT1):c.381C>T (p.Pro127=) rs771681406
NM_024426.6(WT1):c.42C>T (p.Val14=) rs1343194102
NM_024426.6(WT1):c.450C>T (p.Ser150=) rs1213710686
NM_024426.6(WT1):c.480G>A (p.Gln160=) rs758900425
NM_024426.6(WT1):c.498T>C (p.Thr166=) rs1554946487
NM_024426.6(WT1):c.513C>A (p.Gly171=) rs536728682
NM_024426.6(WT1):c.555C>T (p.Phe185=) rs1554946465
NM_024426.6(WT1):c.585C>T (p.Ser195=) rs1332888095
NM_024426.6(WT1):c.609C>T (p.Asn203=) rs2234583
NM_024426.6(WT1):c.633C>T (p.Leu211=) rs576677344
NM_024426.6(WT1):c.75C>T (p.Ser25=) rs1417997475
NM_024426.6(WT1):c.87C>T (p.Cys29=) rs1554946770

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