ClinVar Miner

List of variants reported as likely pathogenic for Familial hypoplastic, glomerulocystic kidney

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Total variants: 10
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HGVS dbSNP
NM_000458.4(HNF1B):c.1006C>T (p.His336Tyr) rs138986885
NM_000458.4(HNF1B):c.1325T>C (p.Met442Thr) rs193922482
NM_000458.4(HNF1B):c.221T>A (p.Leu74Ter) rs193922486
NM_000458.4(HNF1B):c.344G>A (p.Ser115Asn) rs193922487
NM_000458.4(HNF1B):c.345-1G>T rs193922488
NM_000458.4(HNF1B):c.477del (p.Pro159_Met160insTer) rs193922489
NM_000458.4(HNF1B):c.511T>C (p.Trp171Arg) rs193922490
NM_000458.4(HNF1B):c.703C>T (p.Arg235Trp) rs193922491
NM_000458.4(HNF1B):c.949G>T (p.Ala317Ser) rs193922492
NM_000458.4(HNF1B):c.962A>G (p.Asn321Ser) rs193922493

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