List of variants in gene ACADS 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000017.4(ACADS):c.250G>A (p.Val84Met)	rs751283667	0.00006
NM_000017.4(ACADS):c.1156C>T (p.Arg386Cys)	rs537072819	0.00003
NM_000017.4(ACADS):c.1105G>A (p.Gly369Ser)	rs145466253	0.00002
NM_000017.4(ACADS):c.1130C>T (p.Pro377Leu)	rs183161718	0.00001
NM_000017.4(ACADS):c.425C>G (p.Pro142Arg)	rs148297461	0.00001
NM_000017.4(ACADS):c.449G>T (p.Gly150Val)	rs1057524803	0.00001
NM_000017.4(ACADS):c.481A>G (p.Ser161Gly)	rs755856935	0.00001
NM_000017.4(ACADS):c.1054G>A (p.Ala352Thr)	rs202078273
NM_000017.4(ACADS):c.1153G>T (p.Ala385Ser)	rs202124189
NM_000017.4(ACADS):c.154_156del (p.Glu52del)
NM_000017.4(ACADS):c.461T>G (p.Leu154Arg)	rs1057523592
NM_000017.4(ACADS):c.650T>C (p.Met217Thr)	rs1472894784
NM_000017.4(ACADS):c.656C>G (p.Thr219Arg)	rs148588313
NM_000017.4(ACADS):c.721C>A (p.Leu241Ile)
NM_000017.4(ACADS):c.880G>A (p.Ala294Thr)	rs770406570
NM_000017.4(ACADS):c.944_946del (p.Ala315del)	rs1290727105

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