List of variants in gene ACOX1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004035.7(ACOX1):c.*4250T>G	rs112541815	0.01052
NM_004035.7(ACOX1):c.921G>A (p.Arg307=)	rs79677613	0.00869
NM_004035.7(ACOX1):c.*4551C>T	rs139936850	0.00697
NM_004035.7(ACOX1):c.*5134A>G	rs116309575	0.00587
NM_004035.7(ACOX1):c.*2575T>C	rs115141246	0.00429
NM_004035.7(ACOX1):c.954A>G (p.Glu318=)	rs16968343	0.00404
NM_004035.7(ACOX1):c.*1813C>T	rs144899104	0.00228
NM_004035.7(ACOX1):c.*3988A>T	rs149774605	0.00227
NM_004035.7(ACOX1):c.1135_1141del	rs148425334
NM_004035.7(ACOX1):c.*4472dup	rs59512794

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