List of variants in gene ACADM reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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.216+10T>C	rs2275378	0.30596
NM_000016.6(ACADM):c.1161A>G (p.Val387=)	rs1061337	0.23824
NM_000016.6(ACADM):c.119-20T>C	rs74090724	0.05208
NM_000016.6(ACADM):c.351A>C (p.Thr117=)	rs74090726	0.04935
NM_000016.6(ACADM):c.489T>G (p.Pro163=)	rs78392995	0.02010
NM_000016.6(ACADM):c.900C>T (p.Thr300=)	rs17097429	0.01131
NM_000016.6(ACADM):c.469-9A>G	rs181322317	0.00223
NM_000016.6(ACADM):c.678A>G (p.Ala226=)	rs2229249	0.00120
NM_000016.6(ACADM):c.1194+11A>G	rs373059851	0.00084
NM_000016.6(ACADM):c.1194+23del	rs759041992
NM_000016.6(ACADM):c.1194+23dup	rs759041992
NM_000016.6(ACADM):c.1195-8dup	rs764088394

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