Related gene-specific medical variations for Gene (Select 645037) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2604869	NM_001098412.4(GAGE13):c.181G>A (p.Asp61Asn)	GAGE13, GAGE2B +2 more (D60N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2507874	NM_001098412.4(GAGE13):c.320C>G (p.Thr107Arg)	GAGE2B, GAGE2C +1 more (T106R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2475612	NM_001098412.4(GAGE13):c.298C>T (p.Pro100Ser)	GAGE13, GAGE2B +1 more (P99S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2382872	NM_001098412.4(GAGE13):c.79A>G (p.Met27Val)	GAGE2C, GAGE13 +1 more (M27V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2342619	NM_001098412.4(GAGE13):c.289A>G (p.Met97Val)	GAGE2C, GAGE13 +2 more (M96V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2283816	NM_001098412.4(GAGE13):c.208C>T (p.Pro70Ser)	GAGE2D, GAGE2C +2 more (P69S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar