ClinVar Miner

List of variants in gene ANO7 reported as benign by GeneDx

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Gene type:
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Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_001370694.2(ANO7):c.724-11= rs1179530 0.99976
NM_001370694.2(ANO7):c.1972+246C>G rs11678844 0.83639
NM_001370694.2(ANO7):c.2321+131G>A rs11692790 0.82611
NM_001370694.2(ANO7):c.167-261A>G rs12998792 0.82497
NM_001370694.2(ANO7):c.1359+23G>A rs10192730 0.77855
NM_001370694.2(ANO7):c.167-101A>C rs12694996 0.77290
NM_001370694.2(ANO7):c.310-241A>G rs11674264 0.69644
NM_001370694.2(ANO7):c.418-13C>T rs2013250 0.69456
NM_001370694.2(ANO7):c.723C>T (p.Asp241=) rs2074840 0.58740
NM_001370694.2(ANO7):c.1973-298G>A rs56098160 0.55560
NM_001370694.2(ANO7):c.1729-205A>G rs12620606 0.50872
NM_001370694.2(ANO7):c.1078-296A>G rs13021863 0.36277
NM_001370694.2(ANO7):c.-8+266G>A rs11694282 0.34922
NM_001370694.2(ANO7):c.1077+179C>A rs9679681 0.34846
NM_001370694.2(ANO7):c.166+273T>A rs2074837 0.29377
NM_001370694.2(ANO7):c.889+256G>A rs13410224 0.23717
NM_001370694.2(ANO7):c.-7-206C>T rs11683690 0.23187
NM_001370694.2(ANO7):c.1638C>T (p.Tyr546=) rs7593101 0.23100
NM_001370694.2(ANO7):c.9G>T (p.Arg3=) rs11695874 0.22239
NM_001370694.2(ANO7):c.612+15C>G rs78154103 0.20337
NM_001370694.2(ANO7):c.1319C>T (p.Ala440Val) rs57677160 0.20020
NM_001370694.2(ANO7):c.2572G>A (p.Glu858Lys) rs7590653 0.19676
NM_001370694.2(ANO7):c.2412+41G>C rs13392669 0.18432
NM_001370694.2(ANO7):c.1673+128G>C rs7566006 0.18287
NM_001370694.2(ANO7):c.1561+106T>C rs58527121 0.17104
NM_001370694.2(ANO7):c.1827-201C>A rs749264 0.16515
NM_001370694.2(ANO7):c.2113G>A (p.Ala705Thr) rs76832527 0.13055
NM_001370694.2(ANO7):c.108+245A>G rs4675826 0.12757
NM_001370694.2(ANO7):c.1673+171C>G rs62187431 0.12322
NM_001370694.2(ANO7):c.417+74C>T rs34107209 0.11214
NM_001370694.2(ANO7):c.1673+154T>C rs60219972 0.10646
NM_001370694.2(ANO7):c.*259C>T rs61744217 0.10172
NM_001370694.2(ANO7):c.2579_2580del (p.Gly859_Ser860insTer) rs60985508 0.09667
NM_001370694.2(ANO7):c.1359+129A>G rs13401111 0.08980
NM_001370694.2(ANO7):c.1359+191T>C rs13403889 0.07955
NM_001370694.2(ANO7):c.2584-51C>G rs77050519 0.06480
NM_001370694.2(ANO7):c.1078-309C>T rs566270205 0.06383
NM_001370694.2(ANO7):c.*166C>T rs61747382 0.06274
NM_001370694.2(ANO7):c.890-271G>A rs113870213 0.05269
NM_001370694.2(ANO7):c.37G>A (p.Val13Ile) rs2302054 0.05082
NM_001370694.2(ANO7):c.2056A>C (p.Ile686Leu) rs74804606 0.05035
NM_001370694.2(ANO7):c.554+239C>T rs2074839 0.04714
NM_001370694.2(ANO7):c.889+8C>T rs77640154 0.04614
NM_001370694.2(ANO7):c.613-297C>T rs4675823 0.04490
NM_001370694.2(ANO7):c.613-96C>T rs111236002 0.03176
NM_001370694.2(ANO7):c.1561+64C>T rs113377437 0.03109
NM_001370694.2(ANO7):c.2610G>A (p.Thr870=) rs115620538 0.02806
NM_001370694.2(ANO7):c.1142T>A (p.Val381Glu) rs4675982 0.02714
NM_001370694.2(ANO7):c.1077+73C>A rs114496336 0.02468
NM_001370694.2(ANO7):c.889+137C>T rs59218195 0.01703
NM_001370694.2(ANO7):c.-7-27A>G rs2302053 0.00274
NM_001370694.2(ANO7):c.-8+235G>A rs11694278
NM_001370694.2(ANO7):c.1078-310T>C rs4675983
NM_001370694.2(ANO7):c.1078-320C>T rs11674804
NM_001370694.2(ANO7):c.108+183T>G rs4675985
NM_001370694.2(ANO7):c.1973-14C>T rs111770284
NM_001370694.2(ANO7):c.2100G>C (p.Pro700=) rs78605785
NM_001370694.2(ANO7):c.2100G>T (p.Pro700=) rs78605785
NM_001370694.2(ANO7):c.2178+52del rs748712372
NM_001370694.2(ANO7):c.417+214G>A rs35554938
NM_001370694.2(ANO7):c.554+213C>A rs76538371
NM_001370694.2(ANO7):c.555-286C>A rs2011792
NM_001370694.2(ANO7):c.555-55_555-18del rs879293108
NM_001370694.2(ANO7):c.723+207C>T rs2074841
NM_001370694.2(ANO7):c.724-240G>A rs2074842

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