List of variants in gene combination LOC129936730, NDUFAF3 reported as uncertain significance 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_199069.2(NDUFAF3):c.109G>A (p.Ala37Thr)	rs527954570	0.00014
NM_199069.2(NDUFAF3):c.78-15C>G	rs587781096	0.00007

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