List of variants in gene CDH1 reported as likely benign for Hereditary breast ovarian cancer syndrome

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1359C>T (p.His453=)	rs114861467	0.00009
NM_004360.5(CDH1):c.1888C>G (p.Leu630Val)	rs2276331	0.00009
NM_004360.5(CDH1):c.214G>A (p.Asp72Asn)	rs35606263	0.00006

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