List of variants in gene CDH2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001792.5(CDH2):c.399+3A>G	rs200907338	0.00060
NM_001792.5(CDH2):c.865G>A (p.Val289Ile)	rs142589795	0.00038
NM_001792.5(CDH2):c.1499A>G (p.Asn500Ser)	rs201866479	0.00017
NM_001792.5(CDH2):c.173-22589C>T
NM_001792.5(CDH2):c.231A>T (p.Ala77=)	rs148115828

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