ClinVar Miner

List of variants in gene RRM2B reported as likely benign 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015713.5(RRM2B):c.2151_2152insA	rs563908556	0.00332
NM_015713.5(RRM2B):c.3003_3004del	rs552260099

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