List of variants in gene ACADM reported as uncertain significance by GeneDx

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000016.6(ACADM):c.214G>A (p.Glu72Lys)	rs374358376	0.00028
NM_000016.6(ACADM):c.-17C>G	rs367734665	0.00013
NM_000016.6(ACADM):c.1247T>C (p.Ile416Thr)	rs760892123	0.00006
NM_000016.6(ACADM):c.131A>G (p.Gln44Arg)	rs751647383	0.00006
NM_000016.6(ACADM):c.388-5G>A	rs759254037	0.00004
NM_000016.6(ACADM):c.286G>C (p.Gly96Arg)	rs886042055	0.00003
NM_000016.6(ACADM):c.599+3A>G	rs375921211	0.00003
NM_000016.6(ACADM):c.158G>A (p.Arg53His)	rs754938068	0.00002
NM_000016.6(ACADM):c.296G>T (p.Gly99Val)	rs370608001	0.00001
NM_000016.6(ACADM):c.661G>A (p.Gly221Arg)	rs753627680	0.00001
NM_000016.6(ACADM):c.112A>C (p.Ser38Arg)	rs2100347323
NM_000016.6(ACADM):c.1159G>C (p.Val387Leu)	rs1057518630
NM_000016.6(ACADM):c.350C>T (p.Thr117Ile)
NM_000016.6(ACADM):c.514A>G (p.Ile172Val)	rs1179642524
NM_000016.6(ACADM):c.526G>A (p.Ala176Thr)	rs200754053
NM_000016.6(ACADM):c.653C>A (p.Ala218Asp)
NM_000016.6(ACADM):c.683C>A (p.Thr228Asn)	rs149678400
NM_000016.6(ACADM):c.773C>T (p.Pro258Leu)	rs1022879056
NM_000016.6(ACADM):c.866T>C (p.Val289Ala)	rs1057520215

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