List of variants in gene MT-TP reported as uncertain significance 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: 9

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TP):m.15976T>C	rs1603225620
NC_012920.1(MT-TP):m.15983T>C	rs1603225623
NC_012920.1(MT-TP):m.15984T>C	rs1603225624
NC_012920.1(MT-TP):m.15994A>G	rs1603225627
NC_012920.1(MT-TP):m.15995G>A	rs1603225630
NC_012920.1(MT-TP):m.16003T>C	rs1603225634
NC_012920.1(MT-TP):m.16013A>G	rs1603225636
NC_012920.1(MT-TP):m.16018_16032dup	rs1603225639
NC_012920.1(MT-TP):m.16021C>T	rs1603225641

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