Related gene-specific medical variations for Gene (Select 2857) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3101727	NM_001097579.2(GPR34):c.8G>A (p.Ser3Asn)	CASK, GPR34 (S3N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101726	NM_001097579.2(GPR34):c.796C>T (p.Arg266Cys)	CASK, GPR34 (R266C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101725	NM_001097579.2(GPR34):c.599A>G (p.Asn200Ser)	CASK, GPR34 (N200S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466972	NM_001097579.2(GPR34):c.146A>G (p.Asp49Gly)	CASK, GPR34 (D49G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 713839	NM_001097579.2(GPR34):c.888A>G (p.Val296=)	CASK, GPR34	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 235298	NM_001097579.2(GPR34):c.884A>G (p.Asn295Ser)	CASK, GPR34 (N295S)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign/Likely benign

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