List of variants in gene MT-TM studied 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
		ClinVar version:

Total variants: 13

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HGVS	dbSNP
NC_012920.1(MT-CYB):m.4417A>G	rs1603219452
NC_012920.1(MT-CYB):m.4418T>C	rs1556422856
NC_012920.1(MT-CYB):m.4429G>A	rs1603219456
NC_012920.1(MT-CYB):m.4435A>G	rs878930498
NC_012920.1(MT-CYB):m.4437C>T	rs1603219459
NC_012920.1(MT-CYB):m.4451T>G	rs1603219461
NC_012920.1(MT-CYB):m.4452T>C	rs377043134
NC_012920.1(MT-CYB):m.4454T>A	rs11510098
NC_012920.1(MT-CYB):m.4454T>C	rs11510098
NC_012920.1(MT-CYB):m.4455A>G	rs878986264
NC_012920.1(MT-CYB):m.4456C>T	rs1603219465
NC_012920.1(MT-CYB):m.4464G>A	rs1603219466
NC_012920.1(MT-CYB):m.4466A>G	rs1603219467

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