List of variants in gene MT-TD studied 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
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TD):m.7518A>G	rs1603220992
NC_012920.1(MT-TD):m.7520G>A	rs1603220993
NC_012920.1(MT-TD):m.7521G>A	rs200336937
NC_012920.1(MT-TD):m.7525T>C	rs1603220995
NC_012920.1(MT-TD):m.7533C>T	rs1603221000
NC_012920.1(MT-TD):m.7534C>T	rs1603221002
NC_012920.1(MT-TD):m.7538T>C	rs1603221004
NC_012920.1(MT-TD):m.7543A>G	rs1603221006
NC_012920.1(MT-TD):m.7546T>C	rs1603221007
NC_012920.1(MT-TD):m.7547T>C	rs879076142
NC_012920.1(MT-TD):m.7552A>G	rs1603221008
NC_012920.1(MT-TD):m.7555T>C	rs1603221010
NC_012920.1(MT-TD):m.7559A>G	rs1556423308
NC_012920.1(MT-TD):m.7561T>C	rs1603221012
NC_012920.1(MT-TD):m.7562A>G	rs1603221015
NC_012920.1(MT-TD):m.7566G>A	rs1603221016
NC_012920.1(MT-TD):m.7567C>T	rs1603221018
NC_012920.1(MT-TD):m.7568T>C	rs1603221019
NC_012920.1(MT-TD):m.7568dup	rs1603221020
NC_012920.1(MT-TD):m.7569A>G	rs1603221021
NC_012920.1(MT-TD):m.7570A>G	rs1556423311
NC_012920.1(MT-TD):m.7572T>C	rs1603221022
NC_012920.1(MT-TD):m.7576A>G	rs1603221023
NC_012920.1(MT-TD):m.7577T>C	rs1603221025
NC_012920.1(MT-TD):m.7581T>C	rs201582552
NC_012920.1(MT-TD):m.7582C>T	rs1603221026
NC_012920.1(MT-TD):m.7585A>G	rs1603221028

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