List of variants in gene MT-TT reported as likely benign for MELAS syndrome

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	gnomAD frequency
NC_012920.1(MT-CYB):m.15893T>C	rs1603225570
NC_012920.1(MT-CYB):m.15895T>C	rs1603225571
NC_012920.1(MT-CYB):m.15909A>G	rs1556424690
NC_012920.1(MT-CYB):m.15911A>G	rs1603225583
NC_012920.1(MT-CYB):m.15925C>T	rs1603225595
NC_012920.1(MT-CYB):m.15936A>G	rs1556424701
NC_012920.1(MT-CYB):m.15937A>T	rs1603225605
NC_012920.1(MT-CYB):m.15937del	rs1603225604
NC_012920.1(MT-CYB):m.15944T>C	rs1603225608
NC_012920.1(MT-CYB):m.15952C>T	rs1603225613

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