Related gene-specific medical variations for Gene (Select 196883) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3269494	NM_001198568.2(ADCY4):c.59A>G (p.Tyr20Cys)	ADCY4, LOC130055423 (Y20C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269473	NM_001198568.2(ADCY4):c.32C>A (p.Pro11His)	ADCY4, LOC130055423 (P11H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance