List of variants in gene combination LOC129938008, MCCC1 reported as likely benign for 3-methylcrotonyl-CoA carboxylase 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020166.5(MCCC1):c.6G>A (p.Ala2=)	rs768348047	0.00001
NM_020166.5(MCCC1):c.9G>A (p.Ala3=)	rs1191355416	0.00001
NM_020166.5(MCCC1):c.12C>T (p.Ala4=)

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