Related gene-specific medical variations for Gene (Select 9936) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2459104	NM_014880.5(CD302):c.13G>A (p.Ala5Thr)	CD302, LY75-CD302 (A5T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322491	NM_014880.5(CD302):c.20C>G (p.Pro7Arg)	CD302, LY75-CD302 (P7R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2315049	NM_014880.5(CD302):c.17T>G (p.Leu6Arg)	CD302, LY75-CD302 (L6R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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