List of variants in gene CDH1 reported as uncertain significance for Hereditary breast ovarian cancer syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1409C>T (p.Thr470Ile)	rs370864592	0.00012
NM_004360.5(CDH1):c.2494G>A (p.Val832Met)	rs35572355	0.00004
NM_004360.5(CDH1):c.377C>T (p.Pro126Leu)	rs746703615	0.00004
NM_004360.5(CDH1):c.1417G>A (p.Val473Ile)	rs36087757	0.00003
NM_004360.5(CDH1):c.1930G>A (p.Asp644Asn)	rs587781696	0.00002
NM_004360.5(CDH1):c.2638G>A (p.Glu880Lys)	rs34507583	0.00001
NM_004360.5(CDH1):c.1108G>A (p.Asp370Asn)	rs1960859184
NM_004360.5(CDH1):c.1634G>A (p.Arg545Gln)	rs587780115
NM_004360.5(CDH1):c.2218C>T (p.Pro740Ser)	rs773795943
NM_004360.5(CDH1):c.2371C>G (p.Leu791Val)	rs786202598
NM_004360.5(CDH1):c.437C>G (p.Ser146Cys)	rs751425296

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