List of variants in gene ACADM reported as benign by Eurofins Ntd Llc (ga)

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: 6

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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.-34T>C	rs59932454	0.05213
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

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