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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000017.4(ACADS):c.669G>A (p.Thr223=)	rs17848089	0.00056
NM_000017.4(ACADS):c.624+8C>T	rs371550264	0.00039
NM_000017.4(ACADS):c.465C>T (p.Ser155=)	rs141492002	0.00016
NM_000017.4(ACADS):c.825C>T (p.Ile275=)	rs200652158	0.00014
NM_000017.4(ACADS):c.*4C>T	rs774815274	0.00009
NM_000017.4(ACADS):c.1108A>G (p.Met370Val)	rs566325901	0.00009
NM_000017.4(ACADS):c.327C>T (p.Cys109=)	rs144083614	0.00007
NM_000017.4(ACADS):c.624+11C>T	rs763811046	0.00006
NM_000017.4(ACADS):c.1104C>T (p.Gly368=)	rs200165866	0.00004
NM_000017.4(ACADS):c.147C>G (p.Ala49=)	rs202193021	0.00004
NM_000017.4(ACADS):c.473-9T>G	rs751507296	0.00001

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