Variants with conflicting interpretations "pathogenic" from Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine and "uncertain significance" from Baylor Genetics

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:
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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.2890C>T (p.Arg964Cys)	rs201477273	0.00033
NM_002693.3(POLG):c.1156C>T (p.Arg386Cys)	rs199759055	0.00002
NM_001278716.2(FBXL4):c.1652T>A (p.Ile551Asn)	rs1554215979

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