ClinVar Miner

List of variants in gene LOC130067861, SCO2 studied for Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005138.3(SCO2):c.-83A>G	rs886057632	0.00006
NM_005138.3(SCO2):c.-51C>T	rs886057631	0.00001

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