List of variants in gene combination COX15, ENTPD7 reported as benign for Leigh syndrome

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004376.5(COX15):c.*3566C>T	rs2300983	0.84064
NM_078470.6(COX15):c.*3417T>C	rs10883407	0.10248
NM_004376.5(COX15):c.*3268A>C	rs1056844	0.09586

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