List of variants reported as likely benign 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1774G>A (p.Ala592Thr)	rs35187787	0.00311
NM_004360.5(CDH1):c.88C>A (p.Pro30Thr)	rs139866691	0.00129
NM_004360.5(CDH1):c.303C>T (p.Tyr101=)	rs150789339	0.00027
NM_004360.5(CDH1):c.670C>T (p.Arg224Cys)	rs200310662	0.00021
NM_004360.5(CDH1):c.1409C>T (p.Thr470Ile)	rs370864592	0.00012
NM_004360.5(CDH1):c.2512A>G (p.Ser838Gly)	rs121964872	0.00011
NM_004360.5(CDH1):c.48+15_48+16del	rs730881655	0.00006
NM_004360.5(CDH1):c.84C>T (p.Cys28=)	rs587780789	0.00004
NM_004360.5(CDH1):c.1225T>C (p.Trp409Arg)	rs587778176	0.00003
NM_004360.5(CDH1):c.2358C>T (p.Asp786=)	rs760701558	0.00001

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