List of variants in gene MT-TS2 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: 13

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HGVS	dbSNP
NC_012920.1(MT-CYB):m.12215T>C	rs1603223617
NC_012920.1(MT-CYB):m.12216C>T	rs1603223618
NC_012920.1(MT-CYB):m.12217A>G	rs1556424082
NC_012920.1(MT-CYB):m.12223A>G	rs1603223624
NC_012920.1(MT-CYB):m.12234A>G	rs1603223628
NC_012920.1(MT-CYB):m.12235T>C	rs1556424083
NC_012920.1(MT-CYB):m.12237C>T	rs1603223632
NC_012920.1(MT-CYB):m.12239C>T	rs376062400
NC_012920.1(MT-CYB):m.12241del	rs1603223633
NC_012920.1(MT-CYB):m.12245T>C	rs1603223634
NC_012920.1(MT-CYB):m.12246C>T	rs28508189
NC_012920.1(MT-CYB):m.12248A>G	rs202114991
Single allele	rs28359170

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