ClinVar Miner

List of variants in gene combination NDUFA2, TMCO6 reported as uncertain significance for Mitochondrial complex 1 deficiency, nuclear type 13

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002488.5(NDUFA2):c.209-39G>A	rs780685763	0.00019
NM_002488.5(NDUFA2):c.199G>T (p.Ala67Ser)	rs1235620751

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