List of variants in gene ACADM reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000016.6(ACADM):c.994C>T (p.Leu332=)	rs138098371	0.00093
NM_000016.6(ACADM):c.645T>A (p.Ala215=)	rs147395095	0.00079
NM_000016.6(ACADM):c.210T>G (p.Thr70=)	rs778891510	0.00010
NM_000016.6(ACADM):c.286+190T>C	rs750012444	0.00006
NM_000016.6(ACADM):c.57T>C (p.His19=)	rs762984318	0.00004
NM_000016.6(ACADM):c.927C>T (p.Phe309=)	rs771550655	0.00002
NM_000016.6(ACADM):c.286+223C>T	rs755476467	0.00001
NM_000016.6(ACADM):c.495A>G (p.Ala165=)	rs2525608713
NM_000016.6(ACADM):c.945+301C>T

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