List of variants in gene ACADM reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_000016.6(ACADM):c.216+10T>C	rs2275378	0.30596
NM_000016.6(ACADM):c.469-22C>A	rs12127402	0.25202
NM_000016.6(ACADM):c.31-32C>G	rs7524467	0.23867
NM_000016.6(ACADM):c.1161A>G (p.Val387=)	rs1061337	0.23824
NM_000016.6(ACADM):c.-34T>C	rs59932454	0.05213
NM_000016.6(ACADM):c.119-20T>C	rs74090724	0.05208
NM_000016.6(ACADM):c.351A>C (p.Thr117=)	rs74090726	0.05204
NM_000016.6(ACADM):c.*39G>A	rs17848065	0.04004
NM_000016.6(ACADM):c.31-73T>C	rs142795930	0.02211
NM_000016.6(ACADM):c.489T>G (p.Pro163=)	rs78392995	0.02136
NM_000016.6(ACADM):c.*77C>T	rs143911981	0.00652
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.468+71T>C	rs571856182	0.00198
NM_000016.6(ACADM):c.678A>G (p.Ala226=)	rs2229249	0.00108
NM_000016.6(ACADM):c.468+62C>T	rs875989870	0.00019
NM_000016.6(ACADM):c.118+18T>A	rs755405418	0.00003
NM_000016.6(ACADM):c.118+114A>G	rs875989868
NM_000016.6(ACADM):c.118+60del	rs796117827
NM_000016.6(ACADM):c.118+64del	rs875989853

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