ClinVar Miner

List of variants in gene combination MRPL36, NDUFS6 reported as uncertain significance for Mitochondrial complex I 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
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_004553.4(NDUFS6):c.-12C>T	rs145747389	0.01272
NM_004553.6(NDUFS6):c.11C>T (p.Ala4Val)	rs773943416

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