List of variants in gene GCDH reported as benign for glutaryl-CoA dehydrogenase deficiency

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000159.4(GCDH):c.852+223C>T	rs11085825	0.30906
NM_000159.4(GCDH):c.1173G>T (p.Gly391=)	rs1060218	0.30844
NM_000159.4(GCDH):c.1085C>A (p.Ala362Asp)	rs114759170	0.00453
NM_000159.4(GCDH):c.642G>A (p.Thr214=)	rs142806397	0.00170
NM_000159.4(GCDH):c.1197C>T (p.His399=)	rs139344943	0.00131
NM_000159.4(GCDH):c.1011A>G (p.Ala337=)	rs2229460	0.00093
NM_000159.4(GCDH):c.738G>A (p.Ser246=)	rs188548539	0.00023
NM_000159.4(GCDH):c.735C>T (p.Leu245=)	rs372678445	0.00015
NM_000159.4(GCDH):c.886G>A (p.Gly296Ser)	rs539505767	0.00009
NM_000159.4(GCDH):c.801C>T (p.Asp267=)	rs141293881	0.00008
NM_000159.4(GCDH):c.272-12G>A
NM_000159.4(GCDH):c.999G>A (p.Gln333=)	rs878853156

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