List of variants in gene combination ACADM, LOC129930773 reported as likely benign for medium chain acyl-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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000016.6(ACADM):c.30+18G>A	rs762704029
NM_000016.6(ACADM):c.30+18G>C
NM_000016.6(ACADM):c.30+18G>T
NM_000016.6(ACADM):c.30+20T>C	rs1570843347

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