ClinVar Miner

List of variants in gene SCO2 studied for Mitochondrial complex IV deficiency, nuclear type 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005138.2(SCO2):c.-142G>C	rs145052206	0.01794
NM_005138.3(SCO2):c.-114G>C	rs554814235	0.00142
NM_001169109.2(SCO2):c.-14+505G>A	rs375309432	0.00041

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