Related gene-specific medical variations for Gene (Select 5141) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2250239	NM_001111307.2(PDE4A):c.34C>G (p.Leu12Val)	LOC130063497, PDE4A (L12V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 768971	NM_001111307.2(PDE4A):c.60G>C (p.Arg20=)	LOC130063497, PDE4A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 710380	NM_001111307.2(PDE4A):c.51C>T (p.Pro17=)	LOC130063497, PDE4A	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

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