Related gene-specific medical variations for Gene (Select 642517) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2640436	NM_001190810.1(AGAP9):c.742A>G (p.Met248Val)	AGAP9, ANXA8 (M248V)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2356628	NM_001190810.1(AGAP9):c.746G>T (p.Arg249Leu)	AGAP9, ANXA8 (R249L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance