List of variants in gene CDH3 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 35

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HGVS	dbSNP	gnomAD frequency
NM_001793.6(CDH3):c.2281-288T>C	rs3114408	0.97807
NM_001793.6(CDH3):c.161-123T>C	rs3118229	0.89885
NM_001793.6(CDH3):c.1570+297T>G	rs3114401	0.89871
NM_001793.6(CDH3):c.390+37T>C	rs2296410	0.87073
NM_001793.6(CDH3):c.*154G>T	rs1886699	0.85426
NM_001793.6(CDH3):c.720G>A (p.Thr240=)	rs2296409	0.63066
NM_001793.6(CDH3):c.813C>A (p.Thr271=)	rs2296408	0.62977
NM_001793.6(CDH3):c.1424+23A>G	rs2281850	0.62286
NM_001793.6(CDH3):c.1626T>C (p.Asn542=)	rs2296405	0.62283
NM_001793.6(CDH3):c.1571-75G>A	rs2296406	0.62263
NM_001793.6(CDH3):c.997-26T>C	rs1886697	0.61791
NM_001793.6(CDH3):c.1796-137A>G	rs2274240	0.61534
NM_001793.6(CDH3):c.1956G>A (p.Lys652=)	rs2274239	0.61024
NM_001793.6(CDH3):c.2003-182C>A	rs3785135	0.56438
NM_001793.6(CDH3):c.2003-220C>T	rs3785134	0.56425
NM_001793.6(CDH3):c.2134-155C>T	rs2296404	0.55631
NM_001793.6(CDH3):c.2239C>A (p.Arg747=)	rs17715450	0.53279
NM_001793.6(CDH3):c.160+117G>A	rs2236393	0.44521
NM_001793.6(CDH3):c.247-38A>G	rs1952048	0.43462
NM_001793.6(CDH3):c.1183-119T>C	rs4783661	0.38349
NM_001793.6(CDH3):c.1689G>C (p.Gln563His)	rs1126933	0.32131
NM_001793.6(CDH3):c.997-139G>A	rs1886698	0.30861
NM_001793.6(CDH3):c.1570+177C>T	rs3114400	0.20716
NM_001793.6(CDH3):c.692-247G>A	rs57721399	0.18062
NM_001793.6(CDH3):c.692-129G>C	rs112844902	0.05927
NM_001793.6(CDH3):c.1430G>A (p.Arg477His)	rs34494880	0.04895
NM_001793.6(CDH3):c.692-248C>T	rs112314027	0.03589
NM_001793.6(CDH3):c.1257G>A (p.Lys419=)	rs11860187	0.02870
NM_001793.6(CDH3):c.2134-154G>A	rs7185952	0.02785
NM_001793.6(CDH3):c.805A>C (p.Met269Leu)	rs36038900	0.00341
NM_001793.6(CDH3):c.1087C>T (p.Arg363Cys)	rs74026937	0.00225
NM_001793.6(CDH3):c.2003-46A>G	rs8060790
NM_001793.6(CDH3):c.2281-45A>C	rs3114409
NM_001793.6(CDH3):c.247-194del	rs376882052
NM_001793.6(CDH3):c.612C>A (p.Ile204=)	rs8049247

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