ClinVar Miner

List of variants in gene MT-RNR2 reported as uncertain significance by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 3

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.1836A>G	rs878853073
NC_012920.1:m.2483T>C	rs28445203
NC_012920.1:m.3169C>T	rs1057520173

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