ClinVar Miner

List of variants in gene ZNF81 studied for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP
NM_007137.3(ZNF81):c.*1029G>T rs1023977933
NM_007137.3(ZNF81):c.*1050A>G rs539059
NM_007137.3(ZNF81):c.*1170G>T rs565670321
NM_007137.3(ZNF81):c.*1216G>C rs190335043
NM_007137.3(ZNF81):c.*1368C>T rs646881
NM_007137.3(ZNF81):c.*176del rs781900721
NM_007137.3(ZNF81):c.*1782C>T rs782284307
NM_007137.3(ZNF81):c.*2050C>T rs1057515912
NM_007137.3(ZNF81):c.*211G>A rs145662469
NM_007137.3(ZNF81):c.*2171_*2172del rs1057515913
NM_007137.3(ZNF81):c.*2191C>T rs782062721
NM_007137.3(ZNF81):c.*2268del rs1057515914
NM_007137.3(ZNF81):c.*2549A>G rs148356633
NM_007137.3(ZNF81):c.*2605G>A rs782376829
NM_007137.3(ZNF81):c.*2624A>G rs141557587
NM_007137.3(ZNF81):c.*2656T>C rs482066
NM_007137.3(ZNF81):c.*2719C>A rs630493
NM_007137.3(ZNF81):c.*277T>C rs502054
NM_007137.3(ZNF81):c.*284T>C rs187907741
NM_007137.3(ZNF81):c.*2851T>C rs480186
NM_007137.3(ZNF81):c.*2988G>A rs782291969
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.*3879C>G rs782815002
NM_007137.3(ZNF81):c.*3G>A rs1057515907
NM_007137.3(ZNF81):c.*4003G>A rs192009953
NM_007137.3(ZNF81):c.*4053T>G rs5953122
NM_007137.3(ZNF81):c.*4100G>A rs782467926
NM_007137.3(ZNF81):c.*4105C>T rs603691
NM_007137.3(ZNF81):c.*4164A>G rs1057515918
NM_007137.3(ZNF81):c.*4304A>G rs7878660
NM_007137.3(ZNF81):c.*4485G>T rs602251
NM_007137.3(ZNF81):c.*455G>A rs191380891
NM_007137.3(ZNF81):c.*456T>A rs183606613
NM_007137.3(ZNF81):c.*4715C>G rs600999
NM_007137.3(ZNF81):c.*4848G>A rs781982171
NM_007137.3(ZNF81):c.*5062A>G rs140415993
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.*5461G>T rs191181051
NM_007137.3(ZNF81):c.*55C>G rs782807346
NM_007137.3(ZNF81):c.*607A>G rs45588937
NM_007137.3(ZNF81):c.*630A>G rs782306405
NM_007137.3(ZNF81):c.*65A>G rs192847204
NM_007137.3(ZNF81):c.*699C>T rs782777974
NM_007137.3(ZNF81):c.*720A>G rs781983142
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.-146C>T rs116316712
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.147A>G (p.Val49=) rs782661971
NM_007137.3(ZNF81):c.1495A>G (p.Ile499Val) rs182239885
NM_007137.3(ZNF81):c.1539C>A (p.Leu513=) rs186529018
NM_007137.3(ZNF81):c.181+8C>T rs11091216
NM_007137.3(ZNF81):c.18C>T (p.Asp6=) rs145478020
NM_007137.3(ZNF81):c.1911G>A (p.Pro637=) rs663514
NM_007137.3(ZNF81):c.1923C>T (p.Ser641=) rs375228884
NM_007137.3(ZNF81):c.229G>A (p.Glu77Lys) rs201504654
NM_007137.3(ZNF81):c.277+10T>C rs782441233
NM_007137.3(ZNF81):c.350G>T (p.Gly117Val) rs17147793
NM_007137.3(ZNF81):c.417A>G (p.Ile139Met) rs189835360
NM_007137.3(ZNF81):c.470A>G (p.Asn157Ser) rs41312157
NM_007137.3(ZNF81):c.536G>A (p.Ser179Asn) rs28933691
NM_007137.3(ZNF81):c.554C>T (p.Ser185Leu) rs186251256
NM_007137.3(ZNF81):c.638C>A (p.Ala213Glu) rs537825
NM_007137.3(ZNF81):c.8C>T (p.Ala3Val) rs183846665
NM_007137.3(ZNF81):c.999T>C (p.Thr333=) rs369210201

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