List of variants in gene NDUFS6 reported as likely benign for hereditary skeletal muscle disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004553.6(NDUFS6):c.96C>A (p.Val32=)	rs140619622	0.00311
NM_004553.6(NDUFS6):c.117C>G (p.Val39=)	rs556405335	0.00005
NM_004553.6(NDUFS6):c.102G>A (p.Pro34=)	rs763463147	0.00003
NM_004553.6(NDUFS6):c.165G>T (p.Arg55=)	rs147278612	0.00002
NM_004553.6(NDUFS6):c.67C>T (p.Leu23=)	rs1014264454

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