List of variants reported as uncertain significance for Familial cancer of breast; Blepharocheilodontic syndrome 1; Endometrial carcinoma; Hereditary diffuse gastric adenocarcinoma; Ovarian cancer by Fulgent Genetics, Fulgent Genetics

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Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1143G>C (p.Lys381Asn)	rs143727462	0.00012
NM_004360.5(CDH1):c.2644G>A (p.Asp882Asn)	rs200104963	0.00009
NM_004360.5(CDH1):c.1501G>A (p.Val501Met)	rs368690400	0.00004
NM_004360.5(CDH1):c.2336G>A (p.Arg779Gln)	rs587781311	0.00004
NM_004360.5(CDH1):c.499G>A (p.Glu167Lys)	rs769076258	0.00003
NM_004360.5(CDH1):c.1004G>A (p.Arg335Gln)	rs373364873	0.00002
NM_004360.5(CDH1):c.2098C>A (p.Pro700Thr)	rs878854681	0.00002
NM_004360.5(CDH1):c.2558C>T (p.Ser853Leu)	rs569928380	0.00002
NM_004360.5(CDH1):c.1136C>T (p.Thr379Met)	rs587782856	0.00001
NM_004360.5(CDH1):c.1843A>G (p.Ile615Val)	rs1003012321	0.00001
NM_004360.5(CDH1):c.2380G>A (p.Val794Ile)	rs587782466	0.00001
NM_004360.5(CDH1):c.2603G>A (p.Arg868His)	rs369126891	0.00001
NM_004360.5(CDH1):c.322A>G (p.Arg108Gly)	rs587778172	0.00001
NM_004360.5(CDH1):c.1174G>C (p.Val392Leu)	rs141864044
NM_004360.5(CDH1):c.1376T>C (p.Val459Ala)	rs1555516109
NM_004360.5(CDH1):c.1403C>T (p.Thr468Ile)	rs876659141
NM_004360.5(CDH1):c.1430T>C (p.Val477Ala)
NM_004360.5(CDH1):c.1585A>G (p.Thr529Ala)	rs776890776
NM_004360.5(CDH1):c.1649G>C (p.Arg550Thr)	rs771649648
NM_004360.5(CDH1):c.1927A>G (p.Asn643Asp)	rs587781540
NM_004360.5(CDH1):c.2038A>G (p.Thr680Ala)	rs876658936
NM_004360.5(CDH1):c.2116C>G (p.Gln706Glu)
NM_004360.5(CDH1):c.2222T>C (p.Leu741Ser)
NM_004360.5(CDH1):c.2356G>A (p.Asp786Asn)	rs876659218
NM_004360.5(CDH1):c.2578G>C (p.Asp860His)	rs1412506259
NM_004360.5(CDH1):c.2623A>G (p.Met875Val)	rs1555518287
NM_004360.5(CDH1):c.320A>G (p.Tyr107Cys)	rs1060501241
NM_004360.5(CDH1):c.488G>C (p.Cys163Ser)	rs748783182
NM_004360.5(CDH1):c.56C>G (p.Ser19Cys)	rs1221633501
NM_004360.5(CDH1):c.946A>G (p.Met316Val)	rs761182866

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