List of variants in gene RRM2B reported as uncertain significance for Mitochondrial DNA depletion syndrome

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_015713.5(RRM2B):c.*2613del	rs886062563	0.00002
NM_015713.5(RRM2B):c.*2328A>T	rs886062565
NM_015713.5(RRM2B):c.*2492AAGTT[1]	rs886062564
NM_015713.5(RRM2B):c.*74del	rs886062569

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