List of variants in gene MT-CYB reported as uncertain significance for Mitochondrial disease

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: 8

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.14849T>C	rs207460004
NC_012920.1(MT-CYB):m.15117T>C	rs1603225092
NC_012920.1(MT-CYB):m.15192T>G
NC_012920.1(MT-CYB):m.15197T>C	rs207460001
NC_012920.1(MT-CYB):m.15261G>C
NC_012920.1(MT-CYB):m.15467A>G	rs1569484723
NC_012920.1(MT-CYB):m.15579A>G	rs207460002
NC_012920.1(MT-CYB):m.15848A>G	rs1057520206

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