List of variants in gene MT-TI 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: 10

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HGVS	dbSNP
NC_012920.1(MT-CYB):m.4310A>G	rs1556422841
NC_012920.1(MT-CYB):m.4312C>T	rs193303033
NC_012920.1(MT-CYB):m.4313T>C	rs1603219398
NC_012920.1(MT-CYB):m.4314T>A	rs1603219401
NC_012920.1(MT-CYB):m.4314T>C	rs1603219401
NC_012920.1:m.4277T>C	rs876661358
NC_012920.1:m.4316A>G	rs876661360
NC_012920.1:m.4317delA	rs876661361
m.4295A>G	rs121434467
m.4317A>G	rs121434465

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