Related gene-specific medical variations for Gene (Select 388512) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2622602	NM_001204118.2(CLEC17A):c.955G>A (p.Ala319Thr)	ADGRE3, CLEC17A (A319T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2601014	NM_001204118.2(CLEC17A):c.835C>T (p.Arg279Trp)	ADGRE3, CLEC17A (R279W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231052	NM_001204118.2(CLEC17A):c.1103C>T (p.Thr368Met)	ADGRE3, CLEC17A (T368M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2208682	NM_001204118.2(CLEC17A):c.952A>G (p.Arg318Gly)	ADGRE3, CLEC17A (R318G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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