ClinVar Miner

List of variants in gene CDH23 reported as likely benign by GeneDx

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Total variants: 65
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HGVS dbSNP
NM_022124.5(CDH23):c.6713-1036_6713-1034delAGG rs747095097
NM_022124.6(CDH23):c.-15C>A rs760922529
NM_022124.6(CDH23):c.10044C>G (p.Pro3348=) rs370568585
NM_022124.6(CDH23):c.1078C>T (p.Leu360=) rs185917383
NM_022124.6(CDH23):c.1134+22C>T rs115745871
NM_022124.6(CDH23):c.1135-7T>C rs397517303
NM_022124.6(CDH23):c.1206G>A (p.Pro402=) rs397517304
NM_022124.6(CDH23):c.1263C>T (p.Tyr421=)
NM_022124.6(CDH23):c.1291-89C>T
NM_022124.6(CDH23):c.1307G>A (p.Ser436Asn) rs111033369
NM_022124.6(CDH23):c.1423G>A (p.Val475Met) rs62622410
NM_022124.6(CDH23):c.1611C>T (p.Asp537=) rs543225183
NM_022124.6(CDH23):c.1753-7C>T
NM_022124.6(CDH23):c.198G>A (p.Val66=) rs111033288
NM_022124.6(CDH23):c.2176+3G>T rs369606279
NM_022124.6(CDH23):c.2289+3G>A
NM_022124.6(CDH23):c.2290-13del rs397517316
NM_022124.6(CDH23):c.2337G>A (p.Lys779=) rs111033461
NM_022124.6(CDH23):c.2830A>G (p.Ser944Gly) rs188098974
NM_022124.6(CDH23):c.2878G>A (p.Glu960Lys) rs111033458
NM_022124.6(CDH23):c.2970C>T (p.Asp990=) rs56216952
NM_022124.6(CDH23):c.3074G>A (p.Gly1025Asp) rs143179070
NM_022124.6(CDH23):c.4287C>T (p.Pro1429=) rs377493327
NM_022124.6(CDH23):c.429+4G>A rs397517328
NM_022124.6(CDH23):c.4392G>A (p.Ala1464=) rs770421619
NM_022124.6(CDH23):c.4512C>G (p.Thr1504=) rs562273075
NM_022124.6(CDH23):c.4875G>A (p.Val1625=) rs149664909
NM_022124.6(CDH23):c.5022C>T (p.Ile1674=) rs376952695
NM_022124.6(CDH23):c.5026G>A (p.Ala1676Thr) rs56043301
NM_022124.6(CDH23):c.5297T>C (p.Phe1766Ser) rs114745089
NM_022124.6(CDH23):c.5541C>T (p.Asn1847=) rs148632119
NM_022124.6(CDH23):c.5544C>T (p.Asp1848=) rs142131750
NM_022124.6(CDH23):c.5604C>T (p.Ser1868=)
NM_022124.6(CDH23):c.5748C>T (p.Arg1916=) rs568453039
NM_022124.6(CDH23):c.5924-90G>A
NM_022124.6(CDH23):c.5931T>C (p.Pro1977=) rs373457993
NM_022124.6(CDH23):c.6329C>T (p.Ala2110Val) rs111033492
NM_022124.6(CDH23):c.6453C>A (p.Thr2151=) rs369701382
NM_022124.6(CDH23):c.6596T>A (p.Ile2199Asn) rs111033494
NM_022124.6(CDH23):c.6636C>T (p.Val2212=) rs745528904
NM_022124.6(CDH23):c.6687C>T (p.Asp2229=) rs76463072
NM_022124.6(CDH23):c.6713-1058GAG[9] rs747095097
NM_022124.6(CDH23):c.6852G>C (p.Leu2284=) rs56013867
NM_022124.6(CDH23):c.6918G>A (p.Leu2306=) rs146819206
NM_022124.6(CDH23):c.6990G>T (p.Leu2330=) rs111033495
NM_022124.6(CDH23):c.7722C>T (p.Tyr2574=) rs111033483
NM_022124.6(CDH23):c.7762G>C (p.Glu2588Gln) rs41281338
NM_022124.6(CDH23):c.7823G>A (p.Arg2608His) rs202052174
NM_022124.6(CDH23):c.8120_8121delinsTT (p.Pro2707Leu) rs876657422
NM_022124.6(CDH23):c.8283C>T (p.Asn2761=)
NM_022124.6(CDH23):c.8290G>A (p.Val2764Met) rs556148352
NM_022124.6(CDH23):c.832+8A>G rs56129333
NM_022124.6(CDH23):c.8444G>A (p.Arg2815His)
NM_022124.6(CDH23):c.8775C>T (p.Pro2925=) rs766541944
NM_022124.6(CDH23):c.8808C>T (p.Asp2936=) rs148743086
NM_022124.6(CDH23):c.8859C>T (p.Asp2953=) rs11000008
NM_022124.6(CDH23):c.894G>A (p.Leu298=) rs111033474
NM_022124.6(CDH23):c.8980-12C>T rs111583276
NM_022124.6(CDH23):c.9014C>G (p.Ala3005Gly) rs188966938
NM_022124.6(CDH23):c.9077+7C>T rs76114420
NM_022124.6(CDH23):c.9198+9C>T rs546397918
NM_022124.6(CDH23):c.9204G>A (p.Ala3068=) rs192266658
NM_022124.6(CDH23):c.9238G>A (p.Ala3080Thr) rs369395479
NM_022124.6(CDH23):c.9319+18T>C rs1554877902
NM_022124.6(CDH23):c.9320-34C>T

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