List of variants in gene ACADM reported as likely benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_000016.6(ACADM):c.*39G>A	rs17848065	0.04004
NM_000016.6(ACADM):c.469-9A>G	rs181322317	0.00223
NM_000016.6(ACADM):c.1194+11A>G	rs373059851	0.00084
NM_000016.6(ACADM):c.645T>A (p.Ala215=)	rs147395095	0.00079
NM_000016.6(ACADM):c.582C>T (p.Asn194=)	rs778535261	0.00006
NM_000016.6(ACADM):c.600-6T>C	rs771343450	0.00001
NM_000016.6(ACADM):c.610T>C (p.Leu204=)	rs776993753	0.00001
NM_000016.6(ACADM):c.261G>A (p.Met87Ile)	rs1057522841
NM_000016.6(ACADM):c.30+10A>G	rs759413479
NM_000016.6(ACADM):c.61A>C (p.Arg21=)	rs1358331245
NM_000016.6(ACADM):c.708+8A>C	rs372454296
NM_000016.6(ACADM):c.946-9T>C	rs1057524311

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