Related gene-specific medical variations for Gene (Select 8490) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2387305	NM_003617.4(RGS5):c.194T>C (p.Leu65Pro)	RGS5, RGS5-AS1 (L72P +2 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 737960	NM_003617.4(RGS5):c.117G>A (p.Pro39=)	RGS5, RGS5-AS1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GBenign