List of variants in gene ACADM 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_000016.6(ACADM):c.388-284C>T	rs115453910	0.01333
NM_000016.6(ACADM):c.286+44A>C	rs75792854	0.00866
NM_000016.6(ACADM):c.945+262G>A	rs112153756	0.00725
NM_000016.6(ACADM):c.708+299G>T	rs138769157	0.00678
NM_000016.6(ACADM):c.849+228A>G	rs56799454	0.00669
NM_000016.6(ACADM):c.850-79C>G	rs114277271	0.00436
NM_000016.6(ACADM):c.387+40G>A	rs187510227	0.00241
NM_000016.6(ACADM):c.31-37C>T	rs201590881	0.00224
NM_000016.6(ACADM):c.469-9A>G	rs181322317	0.00223
NM_000016.6(ACADM):c.678A>G (p.Ala226=)	rs2229249	0.00108
NM_000016.6(ACADM):c.849+153C>T	rs866000561	0.00106
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.1091T>C (p.Ile364Thr)	rs150710061	0.00031
NM_000016.6(ACADM):c.210T>G (p.Thr70=)	rs778891510	0.00010
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.287-16C>T	rs368504798	0.00003
NM_000016.6(ACADM):c.657T>C (p.Phe219=)	rs758331876	0.00003
NM_000016.6(ACADM):c.120G>A (p.Glu40=)	rs370303161
NM_000016.6(ACADM):c.192T>A (p.Ala64=)	rs1570861432
NM_000016.6(ACADM):c.286+14A>G	rs1570862121
NM_000016.6(ACADM):c.286+190T>C
NM_000016.6(ACADM):c.287-223T>G	rs41291508
NM_000016.6(ACADM):c.849+171_849+172del	rs35897798
NM_000016.6(ACADM):c.945+220dup	rs745487585
NM_000016.6(ACADM):c.945+9A>C	rs768654898
NM_000016.6(ACADM):c.946-7A>T	rs755381568

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