List of variants in gene MT-RNR1 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 28

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.1008A>G	rs727504505
NC_012920.1(MT-CYB):m.1040T>C	rs727503163
NC_012920.1(MT-CYB):m.1041A>G	rs58327546
NC_012920.1(MT-CYB):m.1047A>G	rs1556422506
NC_012920.1(MT-CYB):m.1117A>G	rs2068677687
NC_012920.1(MT-CYB):m.1120C>T	rs727505171
NC_012920.1(MT-CYB):m.1290C>T	rs1556422517
NC_012920.1(MT-CYB):m.1299A>G	rs1556422518
NC_012920.1(MT-CYB):m.953T>C	rs1556422495
NC_012920.1(MT-CYB):m.961_962del	rs1556422498
NC_012920.1(MT-CYB):m.979C>T	rs876657507
NC_012920.1(MT-CYB):m.990T>C	rs727503165
NC_012920.1(MT-ND1):m.1313A>G	rs1603218542
NC_012920.1:m.1341C>T	rs1556422519
NC_012920.1:m.1415G>A	rs876657505
NC_012920.1:m.1461A>G	rs1556422534
NC_012920.1:m.1473C>T	rs1556422538
NC_012920.1:m.1508C>T	rs386828884
NC_012920.1:m.1536A>G	rs876657506
m.1193T>C	rs111033321
m.1211G>A	rs397515725
m.1310C>T	rs111033354
m.951G>A	rs200887992
m.958_960dupCCC	rs111033185
m.960_961insC	rs111033185
m.960delC	rs111033185
m.961T>G	rs3888511
m.980T>C	rs397515731

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