Variants with conflicting interpretations "pathogenic" from Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine and "likely pathogenic" from Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City

Minimum review status of the submission from Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine:		Collection method of the submission from Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_001278716.2(FBXL4):c.219T>A (p.Tyr73Ter)	rs747536886
NM_006567.5(FARS2):c.431A>G (p.Tyr144Cys)	rs397514610

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