List of variants in gene CDH1 reported as pathogenic by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1003C>T (p.Arg335Ter)	rs587780784	0.00001
NM_004360.5(CDH1):c.1147C>T (p.Gln383Ter)	rs587782798
NM_004360.5(CDH1):c.1354_1357del (p.Leu452fs)	rs886039612
NM_004360.5(CDH1):c.2064_2065del (p.Cys688_Glu689delinsTer)	rs587781276
NM_004360.5(CDH1):c.220C>T (p.Arg74Ter)	rs876658932
NM_004360.5(CDH1):c.382del (p.His128fs)	rs1555514492

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