Related gene-specific medical variations for Gene (Select 2868) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282846	NM_182982.3(GRK4):c.541C>G (p.Pro181Ala)	GRK4, LOC126806949 (P149A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597833	NM_182982.3(GRK4):c.644G>T (p.Cys215Phe)	GRK4, LOC129992093 (C183F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595799	NM_182982.3(GRK4):c.548C>G (p.Thr183Arg)	GRK4, LOC126806949 (T183R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553296	NM_182982.3(GRK4):c.677G>A (p.Arg226Lys)	GRK4, LOC129992093 (R32K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332345	NM_182982.3(GRK4):c.1702C>T (p.Pro568Ser)	GRK4, LOC129992097 (P490S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290558	NM_182982.3(GRK4):c.544G>A (p.Val182Ile)	GRK4, LOC126806949 (V150I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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