List of variants in gene MT-TD reported as uncertain significance for MELAS 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: 9

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.7518A>G	rs1603220992
NC_012920.1(MT-CYB):m.7520G>A	rs1603220993
NC_012920.1(MT-CYB):m.7525T>C	rs1603220995
NC_012920.1(MT-CYB):m.7538T>C	rs1603221004
NC_012920.1(MT-CYB):m.7555T>C	rs1603221010
NC_012920.1(MT-CYB):m.7562A>G	rs1603221015
NC_012920.1(MT-CYB):m.7568dup	rs1603221020
NC_012920.1(MT-CYB):m.7577T>C	rs1603221025
NC_012920.1(MT-CYB):m.7582C>T	rs1603221026

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