List of variants in gene MT-TG reported as benign for skeletal muscle disorder

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: 11

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TG):m.10003T>C	rs1603222620
NC_012920.1(MT-TG):m.10005A>G	rs1603222621
NC_012920.1(MT-TG):m.10006A>G	rs1603222622
NC_012920.1(MT-TG):m.10007T>C	rs201906571
NC_012920.1(MT-TG):m.10018A>G	rs1556423757
NC_012920.1(MT-TG):m.10029A>G	rs1603222639
NC_012920.1(MT-TG):m.10031T>C	rs200048690
NC_012920.1(MT-TG):m.10034T>C	rs41347846
NC_012920.1(MT-TG):m.10042A>G	rs1603222643
NC_012920.1(MT-TG):m.10044A>G	rs41362547
NC_012920.1(MT-TG):m.10045T>C	rs1603222648

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