ClinVar Miner

List of variants in gene CDH23 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
Download table as spreadsheet
HGVS dbSNP
NM_022124.6(CDH23):c.10021C>T (p.Arg3341Cys) rs370074117
NM_022124.6(CDH23):c.1301A>G (p.Asn434Ser) rs139287714
NM_022124.6(CDH23):c.1853A>G (p.Tyr618Cys) rs778493031
NM_022124.6(CDH23):c.2236G>A (p.Val746Ile) rs550384315
NM_022124.6(CDH23):c.2263C>T (p.His755Tyr) rs181255269
NM_022124.6(CDH23):c.2330C>A (p.Thr777Lys) rs199709482
NM_022124.6(CDH23):c.2524C>T (p.Arg842Trp) rs368496658
NM_022124.6(CDH23):c.268C>T (p.Arg90Trp) rs1064794990
NM_022124.6(CDH23):c.2854G>A (p.Glu952Lys) rs370554545
NM_022124.6(CDH23):c.3022G>A (p.Val1008Met) rs201053044
NM_022124.6(CDH23):c.3067G>A (p.Asp1023Asn) rs1064796283
NM_022124.6(CDH23):c.3178C>T (p.Arg1060Trp) rs201536811
NM_022124.6(CDH23):c.4405A>G (p.Ile1469Val) rs200635365
NM_022124.6(CDH23):c.4730G>A (p.Arg1577His) rs771464282
NM_022124.6(CDH23):c.4937G>A (p.Gly1646Asp) rs759019656
NM_022124.6(CDH23):c.5647A>C (p.Asn1883His) rs747488431
NM_022124.6(CDH23):c.5945A>G (p.Asn1982Ser) rs555432123
NM_022124.6(CDH23):c.617A>C (p.Asn206Thr) rs528880720
NM_022124.6(CDH23):c.6421A>G (p.Arg2141Gly) rs376414352
NM_022124.6(CDH23):c.6654C>A (p.Asp2218Glu) rs537236734
NM_022124.6(CDH23):c.7379T>G (p.Leu2460Arg) rs1554875886
NM_022124.6(CDH23):c.7465C>G (p.Arg2489Gly) rs754223180
NM_022124.6(CDH23):c.7552G>A (p.Val2518Met) rs376617494
NM_022124.6(CDH23):c.772A>G (p.Ile258Val) rs370782827
NM_022124.6(CDH23):c.8533C>T (p.Arg2845Cys) rs727505254
NM_022124.6(CDH23):c.8729T>C (p.Met2910Thr) rs374171450
NM_022124.6(CDH23):c.8914G>A (p.Glu2972Lys) rs746716712
NM_022124.6(CDH23):c.9569C>T (p.Ala3190Val) rs111033536
NM_022124.6(CDH23):c.9775C>T (p.His3259Tyr) rs1064795569
NM_022124.6(CDH23):c.9928C>T (p.Arg3310Cys) rs200124827

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.