GAPDH[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1262368	NM_002046.7(GAPDH):c.-8C>G	GAPDH	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 3098309	NM_002046.7(GAPDH):c.354G>T (p.Arg118Ser)	GAPDH (R76S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611275	NM_002046.7(GAPDH):c.355G>T (p.Val119Phe)	GAPDH (V77F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508637	NM_002046.7(GAPDH):c.494A>G (p.His165Arg)	GAPDH (H147R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3098310	NM_002046.7(GAPDH):c.755C>G (p.Pro252Arg)	GAPDH (P210R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310091	NM_002046.7(GAPDH):c.968G>A (p.Arg323Lys)	GAPDH (R305K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar