List of variants in gene MT-TY 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: 18

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.5836A>G	rs386828979
NC_012920.1(MT-CYB):m.5837G>A	rs1603220147
NC_012920.1(MT-CYB):m.5839C>T	rs1603220148
NC_012920.1(MT-CYB):m.5840C>A	rs1603220149
NC_012920.1(MT-CYB):m.5840C>T	rs1603220149
NC_012920.1(MT-CYB):m.5841T>C	rs1603220150
NC_012920.1(MT-CYB):m.5846C>T	rs1603220152
NC_012920.1(MT-CYB):m.5852T>C	rs1603220153
NC_012920.1(MT-CYB):m.5855A>G	rs1603220155
NC_012920.1(MT-CYB):m.5858T>C	rs1603220157
NC_012920.1(MT-CYB):m.5864G>A	rs1603220158
NC_012920.1(MT-CYB):m.5865T>C	rs1603220159
NC_012920.1(MT-CYB):m.5867C>T	rs1603220160
NC_012920.1(MT-CYB):m.5875C>T	rs1603220162
NC_012920.1(MT-CYB):m.5876A>G	rs1603220163
NC_012920.1(MT-CYB):m.5885T>C	rs1603220164
NC_012920.1(MT-CYB):m.5889A>G	rs1603220167
m.5843A>G	rs118203894

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