"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "ADCY6"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2683196	NM_015270.5(ADCY6):c.3178G>C (p.Ala1060Pro)	ADCY6, SPMIP11 (A1007P +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1694071	NM_015270.5(ADCY6):c.2833C>G (p.Arg945Gly)	ADCY6 (R892G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1694072	NM_015270.5(ADCY6):c.1999C>A (p.Pro667Thr)	ADCY6 (P667T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1163353	NM_015270.5(ADCY6):c.1904G>A (p.Arg635His)	ADCY6 (R635H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1694073	NM_015270.5(ADCY6):c.1711C>T (p.Arg571Trp)	ADCY6 (R571W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 797997	NM_015270.5(ADCY6):c.1333C>A (p.His445Asn)	ADCY6 (H445N)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1694074	NM_015270.5(ADCY6):c.184C>T (p.Arg62Trp)	ADCY6 (R62W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar