ClinVar Miner

List of variants in gene ZNF41 reported as uncertain significance for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_007130.3(ZNF41):c.*1033A>G rs1057515901
NM_007130.3(ZNF41):c.*469C>T rs1057515902
NM_007130.3(ZNF41):c.-422_-421insGCGCGCACGC rs372112867
NM_007130.3(ZNF41):c.-433_-428GCACGC[3] rs200168272
NM_007130.3(ZNF41):c.-514C>T rs1025319944
NM_007130.3(ZNF41):c.-530G>T rs754233603
NM_007130.3(ZNF41):c.1323C>T (p.Cys441=) rs746076782
NM_007130.3(ZNF41):c.160G>C (p.Asp54His) rs369407023
NM_007130.3(ZNF41):c.281A>G (p.His94Arg) rs779348860
NM_007130.3(ZNF41):c.348C>T (p.Phe116=) rs1057515903

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