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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004376.5(COX15):c.*3661T>C	rs73345141	0.02836
NM_004376.5(COX15):c.*4473T>C	rs10490941	0.01875
NM_004376.5(COX15):c.*4218C>T	rs138423739	0.01377
NM_004376.5(COX15):c.*2640T>G	rs80332976	0.01155

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