List of variants in gene CDH1 reported by University of Washington Department of Laboratory Medicine, University of Washington

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.2295+166C>T	rs143044978	0.00799
NM_004360.5(CDH1):c.1137+86T>G	rs35160345	0.00568
NM_004360.5(CDH1):c.48+105A>G	rs62057828	0.00371
NM_004360.5(CDH1):c.1937-423G>A	rs144719031	0.00304
NM_004360.5(CDH1):c.1680G>C (p.Thr560=)	rs35741240	0.00261
NM_004360.5(CDH1):c.388-1619G>A	rs187126626	0.00225
NM_004360.5(CDH1):c.48+203C>T	rs112622910	0.00195
NM_004360.5(CDH1):c.2413G>A (p.Asp805Asn)	rs200894246	0.00026
NM_004360.5(CDH1):c.2512A>G (p.Ser838Gly)	rs121964872	0.00011
NM_004360.5(CDH1):c.2343A>T (p.Glu781Asp)	rs587780119	0.00006
NM_004360.5(CDH1):c.184G>A (p.Gly62Ser)	rs587781898	0.00003
NM_004360.5(CDH1):c.387+1G>A	rs587781919	0.00001
NM_004360.5(CDH1):c.388-3020G>T	rs559645609	0.00001
NM_004360.5(CDH1):c.1064del (p.Gly354_Leu355insTer)	rs1555515731
NM_004360.5(CDH1):c.1505del (p.Gly502fs)	rs869312765
NM_004360.5(CDH1):c.1937-383A>G	rs869312792
NM_004360.5(CDH1):c.715G>A (p.Gly239Arg)	rs587780537

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