ClinVar Miner

List of variants in gene CDH23 reported as benign by GeneDx

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Gene type:
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Total variants: 69
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HGVS dbSNP
NC_000010.11:g.71511238A>G
NC_000010.11:g.71679344T>C
NC_000010.11:g.71695551T>C
NC_000010.11:g.71739804C>G
NC_000010.11:g.71784847T>C
NC_000010.11:g.71799470C>T
NM_022124.6(CDH23):c.-45_-41AGGCG[2] rs71012280
NM_022124.6(CDH23):c.-5-251A>G
NM_022124.6(CDH23):c.-5-83C>A
NM_022124.6(CDH23):c.1038G>A (p.Pro346=) rs74608315
NM_022124.6(CDH23):c.1053C>T (p.Ser351=) rs7903475
NM_022124.6(CDH23):c.1096G>A (p.Ala366Thr) rs143282422
NM_022124.6(CDH23):c.1134+164C>G
NM_022124.6(CDH23):c.1135-128A>G
NM_022124.6(CDH23):c.1290+217T>C
NM_022124.6(CDH23):c.1449+130T>C rs2305209
NM_022124.6(CDH23):c.145+135C>T
NM_022124.6(CDH23):c.146-125T>C
NM_022124.6(CDH23):c.1515-193A>G
NM_022124.6(CDH23):c.1515-341T>A
NM_022124.6(CDH23):c.1752+110T>C
NM_022124.6(CDH23):c.1753-78A>T
NM_022124.6(CDH23):c.2059+79C>T
NM_022124.6(CDH23):c.2060-19C>G rs2290024
NM_022124.6(CDH23):c.2289+135C>T
NM_022124.6(CDH23):c.2289+240T>C
NM_022124.6(CDH23):c.2290-240C>G
NM_022124.6(CDH23):c.2290-267C>T
NM_022124.6(CDH23):c.2290-268G>A
NM_022124.6(CDH23):c.2424G>A (p.Gly808=) rs76601590
NM_022124.6(CDH23):c.2568C>G (p.Ile856Met) rs188498736
NM_022124.6(CDH23):c.2734-17C>T rs79742451
NM_022124.6(CDH23):c.2953+146C>T
NM_022124.6(CDH23):c.2958G>A (p.Leu986=) rs74702249
NM_022124.6(CDH23):c.3009T>C (p.Ser1003=) rs10823829
NM_022124.6(CDH23):c.4210-7C>T rs79271090
NM_022124.6(CDH23):c.4299T>A (p.Pro1433=) rs12218559
NM_022124.6(CDH23):c.4310G>A (p.Arg1437Gln) rs56181447
NM_022124.6(CDH23):c.4341T>C (p.Asp1447=) rs12218564
NM_022124.6(CDH23):c.4359+11G>A rs12242607
NM_022124.6(CDH23):c.4359+240A>G
NM_022124.6(CDH23):c.4360-333T>C
NM_022124.6(CDH23):c.4488+298G>A
NM_022124.6(CDH23):c.4509C>T (p.Gly1503=) rs10999978
NM_022124.6(CDH23):c.4617+154C>T
NM_022124.6(CDH23):c.4618-77C>T
NM_022124.6(CDH23):c.4846-135C>T
NM_022124.6(CDH23):c.4846-19G>C rs80261750
NM_022124.6(CDH23):c.5100C>T (p.Tyr1700=) rs10762480
NM_022124.6(CDH23):c.5187+73C>T
NM_022124.6(CDH23):c.5411G>A (p.Arg1804Gln) rs3802711
NM_022124.6(CDH23):c.5418C>G (p.Asp1806Glu) rs74145660
NM_022124.6(CDH23):c.5821-309G>A
NM_022124.6(CDH23):c.6130G>A (p.Glu2044Lys) rs10466026
NM_022124.6(CDH23):c.6197G>A (p.Arg2066Gln) rs201887949
NM_022124.6(CDH23):c.6249G>A (p.Pro2083=) rs55964031
NM_022124.6(CDH23):c.6492C>T (p.Ile2164=) rs41281332
NM_022124.6(CDH23):c.67+12C>T rs74144963
NM_022124.6(CDH23):c.6830-81G>A
NM_022124.6(CDH23):c.6847G>A (p.Val2283Ile) rs41281334
NM_022124.6(CDH23):c.7073G>A (p.Arg2358Gln) rs4747194
NM_022124.6(CDH23):c.7139C>T (p.Pro2380Leu) rs4747195
NM_022124.6(CDH23):c.7467C>T (p.Arg2489=) rs111033289
NM_022124.6(CDH23):c.754-254T>C
NM_022124.6(CDH23):c.7572G>A (p.Ala2524=) rs10823849
NM_022124.6(CDH23):c.8980-14C>A rs45522532
NM_022124.6(CDH23):c.9015G>A (p.Ala3005=) rs376497158
NM_022124.6(CDH23):c.9077+8G>A rs11818398
NM_022124.6(CDH23):c.9320-93C>G

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