ClinVar Miner

List of variants in gene ZNF81 reported as uncertain significance for X-linked disease

Included ClinVar conditions (311):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_007137.3(ZNF81):c.*1029G>T rs1023977933
NM_007137.3(ZNF81):c.*1170G>T rs565670321
NM_007137.3(ZNF81):c.*176del rs781900721
NM_007137.3(ZNF81):c.*2050C>T rs1057515912
NM_007137.3(ZNF81):c.*2171_*2172del rs1057515913
NM_007137.3(ZNF81):c.*2268del rs1057515914
NM_007137.3(ZNF81):c.*3399T>A rs1057515915
NM_007137.3(ZNF81):c.*3474T>C rs879956981
NM_007137.3(ZNF81):c.*3525A>C rs782299682
NM_007137.3(ZNF81):c.*3640A>G rs781963956
NM_007137.3(ZNF81):c.*3674C>T rs922923130
NM_007137.3(ZNF81):c.*3G>A rs1057515907
NM_007137.3(ZNF81):c.*4164A>G rs1057515918
NM_007137.3(ZNF81):c.*5127G>C rs1057515919
NM_007137.3(ZNF81):c.*5212A>G rs1057515920
NM_007137.3(ZNF81):c.*5311G>A rs1017729265
NM_007137.3(ZNF81):c.*5422A>G rs1026039563
NM_007137.3(ZNF81):c.*802C>T rs944828411
NM_007137.3(ZNF81):c.*975C>G rs1057515910
NM_007137.3(ZNF81):c.-116A>G rs1057515906
NM_007137.3(ZNF81):c.1080C>T (p.Cys360=) rs377731546
NM_007137.3(ZNF81):c.130C>T (p.Arg44Cys) rs782012314
NM_007137.3(ZNF81):c.277+10T>C rs782441233
NM_007137.3(ZNF81):c.536G>A (p.Ser179Asn) rs28933691
NM_007137.3(ZNF81):c.999T>C (p.Thr333=) rs369210201

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