List of variants in gene MT-TQ reported as benign for Juvenile myopathy, encephalopathy, lactic acidosis AND stroke

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: 17

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HGVS	dbSNP
NC_012920.1(MT-CYB):m.4335C>T	rs878959563
NC_012920.1(MT-CYB):m.4340A>G	rs1603219416
NC_012920.1(MT-CYB):m.4343A>G	rs386828939
NC_012920.1(MT-CYB):m.4350C>T	rs1603219418
NC_012920.1(MT-CYB):m.4353T>C	rs1603219419
NC_012920.1(MT-CYB):m.4370T>C	rs1603219427
NC_012920.1(MT-CYB):m.4371T>C	rs1603219428
NC_012920.1(MT-CYB):m.4373T>C	rs1603219432
NC_012920.1(MT-CYB):m.4381A>G	rs1603219434
NC_012920.1(MT-CYB):m.4384T>C	rs1603219436
NC_012920.1(MT-CYB):m.4385A>T	rs386828941
NC_012920.1(MT-CYB):m.4386T>C	rs1569483940
NC_012920.1(MT-CYB):m.4394C>A	rs1603219441
NC_012920.1(MT-CYB):m.4395A>G	rs1603219443
NC_012920.1:m.4363T>C	rs200009705
Single allele	rs375986475
m.4336T>C	rs41456348

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