Related gene-specific medical variations for Gene (Select 57600) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3279442	NM_020840.3(FNIP2):c.3287C>T (p.Pro1096Leu)	FNIP2, SPMIP2 (P1096L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352208	NM_020840.3(FNIP2):c.3184A>G (p.Met1062Val)	FNIP2, SPMIP2 (M1085V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance