List of variants in gene ACADVL reported as likely benign for not provided

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.879-79T>C	rs114612853	0.00484
NM_000018.4(ACADVL):c.478-196A>C	rs149152410	0.00336
NM_000018.4(ACADVL):c.1839G>A (p.Arg613=)	rs79125791	0.00254
NM_000018.4(ACADVL):c.1844G>A (p.Arg615Gln)	rs148584617	0.00244
NM_000018.4(ACADVL):c.1752-36G>A	rs200709964	0.00173
NM_000018.4(ACADVL):c.1678+23C>T	rs147546456	0.00163
NM_000018.4(ACADVL):c.663C>T (p.Ser221=)	rs144255994	0.00116
NM_000018.4(ACADVL):c.780G>A (p.Thr260=)	rs140871321	0.00108
NM_000018.4(ACADVL):c.1284G>A (p.Lys428=)	rs35501596	0.00061
NM_000018.4(ACADVL):c.1824C>T (p.Ile608=)	rs146115467	0.00058
NM_000018.4(ACADVL):c.1473A>G (p.Leu491=)	rs150518187	0.00051
NM_000018.4(ACADVL):c.1581G>A (p.Pro527=)	rs149436747	0.00035
NM_000018.4(ACADVL):c.*8C>T	rs370513576	0.00011
NM_000018.4(ACADVL):c.255T>C (p.Asp85=)	rs201085520	0.00004
NM_000018.4(ACADVL):c.1828-20C>T	rs757145035	0.00003
NM_000018.4(ACADVL):c.369C>T (p.Asp123=)	rs374524648	0.00003
NM_000018.4(ACADVL):c.957G>A (p.Ser319=)	rs143870522	0.00002
NM_000018.4(ACADVL):c.963C>T (p.Asn321=)	rs568118142	0.00002
NM_000018.4(ACADVL):c.1575C>A (p.Val525=)	rs745996278	0.00001
NM_000018.4(ACADVL):c.480C>T (p.Tyr160=)	rs371910495	0.00001
NM_000018.4(ACADVL):c.864C>T (p.Phe288=)	rs753748672	0.00001
NM_000018.4(ACADVL):c.1434+14T>A	rs202217537
NM_000018.4(ACADVL):c.1605+7G>C	rs572010910
NM_000018.4(ACADVL):c.278-31_278-18del	rs2071164779
NM_000018.4(ACADVL):c.477+50A>T	rs150033153
NM_000018.4(ACADVL):c.753-27C>T	rs374911841
NM_000018.4(ACADVL):c.855G>A (p.Glu285=)	rs201509063
NM_000018.4(ACADVL):c.879-159C>G	rs74562836

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