Related gene-specific medical variations for Gene (Select 55259) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3110768	NM_001366544.2(IRAG2):c.1493C>T (p.Pro498Leu)	DNAI7, IRAG2 (P1445L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3110767	NM_001366544.2(IRAG2):c.1490C>T (p.Pro497Leu)	DNAI7, IRAG2 (P444L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3110766	NM_001366544.2(IRAG2):c.1421A>G (p.Gln474Arg)	DNAI7, IRAG2 (Q421R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2588011	NM_001366544.2(IRAG2):c.1408G>A (p.Ala470Thr)	DNAI7, IRAG2 (A1417T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485725	NM_001366544.2(IRAG2):c.1394A>G (p.Lys465Arg)	DNAI7, IRAG2 (K465R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2469999	NM_001366544.2(IRAG2):c.1333A>G (p.Ile445Val)	DNAI7, IRAG2 (I1392V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign

ClinVar