ClinVar Miner

List of variants in gene combination LOC129931761, NDUFS2 reported as benign for Mitochondrial complex 1 deficiency, nuclear type 6

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_001377299.1(NDUFS2):c.95+9G>C	rs377100925	0.00006
NM_001377299.1(NDUFS2):c.58C>A (p.Pro20Thr)	rs11538340

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