List of variants in gene MT-TV 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: 12

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.1608G>A	rs1603218582
NC_012920.1(MT-CYB):m.1619_1620insT	rs1603218585
NC_012920.1(MT-CYB):m.1629A>G	rs1603218587
NC_012920.1(MT-CYB):m.1630A>G	rs1603218588
NC_012920.1(MT-CYB):m.1631C>T	rs1603218590
NC_012920.1(MT-CYB):m.1636A>G	rs1603218591
NC_012920.1(MT-CYB):m.1638T>C	rs1603218592
NC_012920.1(MT-CYB):m.1641G>A	rs28416113
NC_012920.1(MT-CYB):m.1643A>G	rs1603218595
NC_012920.1(MT-CYB):m.1654T>C	rs1603218602
NC_012920.1(MT-CYB):m.1658T>C	rs1603218607
NC_012920.1(MT-ND1):m.1616A>G	rs2124591018

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