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

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.2474C>T (p.Pro825Leu)	rs587781312	0.00004
NM_004360.5(CDH1):c.377C>T (p.Pro126Leu)	rs746703615	0.00004
NM_004360.5(CDH1):c.2371C>T (p.Leu791Phe)	rs786202598	0.00002
NM_004360.5(CDH1):c.2595G>C (p.Trp865Cys)	rs778019174	0.00002
NM_004360.5(CDH1):c.1171G>A (p.Val391Ile)	rs556110297	0.00001
NM_004360.5(CDH1):c.1250A>G (p.Asn417Ser)	rs773441320	0.00001
NM_004360.5(CDH1):c.1370C>T (p.Thr457Met)	rs587778170	0.00001
NM_004360.5(CDH1):c.1843A>G (p.Ile615Val)	rs1003012321	0.00001
NM_004360.5(CDH1):c.2398C>T (p.Arg800Cys)	rs587782162	0.00001
NM_004360.5(CDH1):c.631A>G (p.Thr211Ala)	rs587781766	0.00001
NM_004360.5(CDH1):c.1234G>A (p.Val412Ile)	rs587782189
NM_004360.5(CDH1):c.1492G>A (p.Asp498Asn)	rs2152135021
NM_004360.5(CDH1):c.1741C>T (p.Leu581Phe)	rs1567512154
NM_004360.5(CDH1):c.1774G>T (p.Ala592Ser)	rs35187787
NM_004360.5(CDH1):c.202T>G (p.Tyr68Asp)	rs1060501218
NM_004360.5(CDH1):c.2435A>G (p.Asp812Gly)	rs878854684

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