Variants in gene ACADM with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_000016.6(ACADM):c.469-9A>G	rs181322317	0.00223
NM_000016.6(ACADM):c.127G>A (p.Glu43Lys)	rs147559466	0.00210
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.666C>A (p.Phe222Leu)	rs139457557	0.00051
NM_000016.6(ACADM):c.1091T>C (p.Ile364Thr)	rs150710061	0.00031
NM_000016.6(ACADM):c.210T>G (p.Thr70=)	rs778891510	0.00010
NM_000016.6(ACADM):c.582C>T (p.Asn194=)	rs778535261	0.00006
NM_000016.6(ACADM):c.287-10G>C	rs368875210	0.00004
NM_000016.6(ACADM):c.57T>C (p.His19=)	rs762984318	0.00004
NM_000016.6(ACADM):c.276A>G (p.Pro92=)	rs1212443202	0.00002
NM_000016.6(ACADM):c.927C>T (p.Phe309=)	rs771550655	0.00002
NM_000016.6(ACADM):c.624T>C (p.Asp208=)	rs886046523

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