List of variants in gene combination COQ6, ENTPD5 reported as pathogenic for not provided

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_182476.3(COQ6):c.782C>T (p.Pro261Leu)	rs371260604	0.00011
NM_182476.3(COQ6):c.349C>T (p.Arg117Ter)	rs376848848	0.00004
NM_182476.3(COQ6):c.1027C>T (p.Arg343Ter)	rs559873718	0.00001
NM_182476.3(COQ6):c.1153_1154del (p.Asp385fs)	rs1064796212
NM_182476.3(COQ6):c.456del (p.Thr153fs)
NM_182476.3(COQ6):c.804del (p.Leu269fs)	rs2140404355
NM_182476.3(COQ6):c.859del (p.Glu287fs)
NM_182476.3(COQ6):c.879del (p.Asn294fs)	rs2140404882

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