ClinVar Miner

List of variants in gene WT1 reported as likely pathogenic for Nephrotic syndrome, type 4

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Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_024426.6(WT1):c.1259A>C (p.His420Pro) rs1554939785
NM_024426.6(WT1):c.1268A>G (p.Glu423Gly) rs2132921573
NM_024426.6(WT1):c.1322A>T (p.Asp441Val) rs2132920206
NM_024426.6(WT1):c.1367T>G (p.Phe456Cys) rs2494732361
NM_024426.6(WT1):c.1384C>T (p.Gln462Ter) rs2132914929
NM_024426.6(WT1):c.1388G>A (p.Arg463Gln) rs1037084691
NM_024426.6(WT1):c.1394T>C (p.Phe465Ser) rs2132914663
NM_024426.6(WT1):c.1399C>T (p.Arg467Trp) rs121907900
NM_024426.6(WT1):c.1400G>A (p.Arg467Gln) rs121907903
NM_024426.6(WT1):c.1447+4C>T rs587776577
NM_024426.6(WT1):c.1504G>C (p.Asp502His) rs2132898667
NM_024426.6(WT1):c.896T>A (p.Leu299Ter) rs2494370978

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