Variants in gene ACADS with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (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: 4

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HGVS	dbSNP	gnomAD frequency
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.663G>T (p.Gly221=)	rs751023929	0.00004
NM_000017.4(ACADS):c.516C>T (p.Ala172=)	rs531683812

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