ClinVar Miner

List of variants in gene CDH3 reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
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.1626T>C (p.Asn542=) rs2296405 0.62283
NM_001793.6(CDH3):c.1956G>A (p.Lys652=) rs2274239 0.61024
NM_001793.6(CDH3):c.2239C>A (p.Arg747=) rs17715450 0.53279
NM_001793.6(CDH3):c.1689G>C (p.Gln563His) rs1126933 0.32131
NM_001793.6(CDH3):c.1430G>A (p.Arg477His) rs34494880 0.04895
NM_001793.6(CDH3):c.1257G>A (p.Lys419=) rs11860187 0.02870
NM_001793.6(CDH3):c.1285G>A (p.Val429Ile) rs34394404 0.00905
NM_001793.6(CDH3):c.2280+7C>T rs114709429 0.00779
NM_001793.6(CDH3):c.996+13C>T rs114408705 0.00573
NM_001793.6(CDH3):c.2058C>T (p.Pro686=) rs116035854 0.00373
NM_001793.6(CDH3):c.805A>C (p.Met269Leu) rs36038900 0.00341
NM_001793.6(CDH3):c.1500C>T (p.Thr500=) rs35232945 0.00241
NM_001793.6(CDH3):c.1087C>T (p.Arg363Cys) rs74026937 0.00225
NM_001793.6(CDH3):c.1236C>T (p.Asn412=) rs186599732 0.00111
NM_001793.6(CDH3):c.345T>C (p.Ser115=) rs138829996 0.00090
NM_001793.6(CDH3):c.141C>G (p.Pro47=) rs74619658 0.00086
NM_001793.6(CDH3):c.909G>T (p.Met303Ile) rs148535251 0.00061
NM_001793.6(CDH3):c.868-17C>T rs141338577 0.00059
NM_001793.6(CDH3):c.1568A>G (p.Asn523Ser) rs191805535 0.00024
NM_001793.6(CDH3):c.582A>C (p.Ser194=) rs148063369 0.00009
NM_001793.6(CDH3):c.2115G>A (p.Gly705=) rs200124759 0.00007
NM_001793.6(CDH3):c.1704G>A (p.Thr568=) rs561193756 0.00006
NM_001793.6(CDH3):c.1776G>A (p.Thr592=) rs766163524 0.00006
NM_001793.6(CDH3):c.109A>T (p.Thr37Ser) rs374627741 0.00004
NM_001793.6(CDH3):c.2133+14_2133+22del rs569391693
NM_001793.6(CDH3):c.612C>A (p.Ile204=) rs8049247

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