List of variants in gene NDUFA10 reported as likely pathogenic for not provided

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004544.4(NDUFA10):c.1000-3C>G	rs199648872	0.00002
NM_004544.4(NDUFA10):c.296G>A (p.Gly99Glu)	rs771444488	0.00001
NM_004544.4(NDUFA10):c.415C>T (p.Arg139Cys)
NM_004544.4(NDUFA10):c.548-2A>G	rs1553573286

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