C1708349[trait identifier] AND "Center for Genomic Medicine, King Fais - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 188085	NM_004360.5(CDH1):c.1679C>T (p.Thr560Met)	CDH1 (T560M +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +4 more	GUncertain significance
Select item 3064696	NM_004360.5(CDH1):c.1697T>G (p.Ile566Arg)	CDH1 (I505R +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance