List of variants in gene COX15 reported as benign 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: 20

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HGVS	dbSNP	gnomAD frequency
NM_078470.6(COX15):c.832+138_832+139dup	rs3832650	0.89215
NM_078470.6(COX15):c.*809G>A	rs7073616	0.86016
NM_078470.6(COX15):c.*1126T>C	rs2231687	0.83974
NM_078470.6(COX15):c.832+194A>C	rs3740077	0.27440
NM_078470.6(COX15):c.832+194_832+195insC	rs56288771	0.27169
NM_078470.6(COX15):c.1102-24A>G	rs11190255	0.25792
NM_078470.6(COX15):c.91-249A>T	rs75829740	0.02254
NM_078470.6(COX15):c.395+97G>A	rs2231681	0.01585
NM_078470.6(COX15):c.1209T>C (p.Asn403=)	rs34652235	0.01341
NM_078470.6(COX15):c.548G>A (p.Arg183His)	rs35483721	0.00915
NM_078470.6(COX15):c.-23G>T	rs2231678	0.00765
NM_078470.6(COX15):c.582+14A>G	rs79410539	0.00263
NM_078470.6(COX15):c.395+20_395+26del	rs774517968	0.00101
NM_078470.6(COX15):c.272+90_272+93del	rs35588478
NM_078470.6(COX15):c.272+91_272+93del	rs35588478
NM_078470.6(COX15):c.272+93del	rs35588478
NM_078470.6(COX15):c.582+62dup	rs5787356
NM_078470.6(COX15):c.832+193_832+194insC	rs201574874
NM_078470.6(COX15):c.987+101dup	rs3215694
NM_078470.6(COX15):c.988-8C>A	rs542092025

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