List of variants in gene 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)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_004553.6(NDUFS6):c.*46C>T	rs145407020	0.00336
NM_004553.6(NDUFS6):c.*15C>T	rs200445799	0.00096
NM_004553.6(NDUFS6):c.198C>T (p.Asn66=)	rs140887831	0.00021
NM_004553.6(NDUFS6):c.*27A>G	rs370587409	0.00014
NM_004553.6(NDUFS6):c.25C>T (p.Arg9Trp)	rs376509886	0.00013
NM_004553.6(NDUFS6):c.*99G>C	rs994577006	0.00012
NM_004553.6(NDUFS6):c.31C>G (p.Leu11Val)	rs755222875	0.00011
NM_004553.6(NDUFS6):c.155G>C (p.Arg52Thr)	rs768060274	0.00006
NM_004553.6(NDUFS6):c.24C>T (p.Cys8=)	rs886060511	0.00003
NM_004553.6(NDUFS6):c.27G>C (p.Arg9=)	rs886060512	0.00001
NM_004553.6(NDUFS6):c.369C>T (p.His123=)	rs745565855

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