Variants in gene ACADS with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000017.4(ACADS):c.625G>A (p.Gly209Ser)	rs1799958	0.20617
NM_000017.4(ACADS):c.511C>T (p.Arg171Trp)	rs1800556	0.03280
NM_000017.4(ACADS):c.625-83G>A	rs150191962	0.01034
NM_000017.4(ACADS):c.796-14G>C	rs201420791	0.00256
NM_000017.4(ACADS):c.522C>T (p.Gly174=)	rs143925225	0.00169
NM_000017.4(ACADS):c.654A>C (p.Pro218=)	rs149430391	0.00075
NM_000017.4(ACADS):c.465C>T (p.Ser155=)	rs141492002	0.00016
NM_000017.4(ACADS):c.1108A>G (p.Met370Val)	rs566325901	0.00009
NM_000017.4(ACADS):c.147C>G (p.Ala49=)	rs202193021	0.00004

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