ClinVar Miner

List of variants in gene MT-TR reported as likely pathogenic 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: 3

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TR):m.10406G>A	rs1603222826
NC_012920.1(MT-TR):m.10408T>C	rs1603222827
NC_012920.1(MT-TR):m.10460T>C	rs1603222848

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