ClinVar Miner

List of variants in gene WDR35 reported as pathogenic for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_001006657.1(WDR35):c.1210dup (p.Glu404Glyfs)
NM_001006657.1(WDR35):c.1414C>T (p.Arg472Ter)
NM_001006657.1(WDR35):c.143-18T>A rs1553324519
NM_001006657.1(WDR35):c.1433+3A>G rs776631281
NM_001006657.1(WDR35):c.1579C>T (p.Gln527Ter)
NM_001006657.1(WDR35):c.1592T>C (p.Leu531Pro) rs397515533
NM_001006657.1(WDR35):c.1633C>T (p.Arg545Ter) rs387907085
NM_001006657.1(WDR35):c.1877A>G (p.Glu626Gly) rs267607174
NM_001006657.1(WDR35):c.1922T>G (p.Leu641Ter) rs199952377
NM_001006657.1(WDR35):c.206G>A (p.Gly69Asp) rs765513105
NM_001006657.1(WDR35):c.25-2A>C rs397515534
NM_001006657.1(WDR35):c.25-2A>G rs397515534
NM_001006657.1(WDR35):c.2522A>T (p.Asp841Val) rs1553316926
NM_001006657.1(WDR35):c.2623G>A (p.Ala875Thr) rs267607175
NM_001006657.1(WDR35):c.2891del (p.Pro964Leufs) rs397515334
NM_001006657.1(WDR35):c.2912A>G (p.Tyr971Cys) rs397515535
NM_001006657.1(WDR35):c.3031G>T (p.Glu1011Ter) rs886043316
NM_001006657.1(WDR35):c.3091C>T (p.His1031Tyr) rs1553316264
NM_001006657.1(WDR35):c.3203A>G (p.Tyr1068Cys) rs541910371
NM_001006657.1(WDR35):c.3459G>T (p.Trp1153Cys) rs1553313859
NM_001006657.1(WDR35):c.504T>A (p.Ser168Arg) rs397515536
NM_001006657.1(WDR35):c.781T>C (p.Trp261Arg) rs431905505
NM_001006657.1(WDR35):c.932G>T (p.Trp311Leu) rs200649783
NM_001006657.1(WDR35):c.994C>T (p.Arg332Ter)
NM_020779.3(WDR35):c.307+214_436+1120del

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