Variants with conflicting interpretations "pathogenic" from Codex Genetics Limited and "uncertain significance" from any submitter

Minimum review status of the submission from Codex Genetics Limited:		Collection method of the submission from Codex Genetics Limited:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_198578.4(LRRK2):c.7153G>A (p.Gly2385Arg)	rs34778348	0.00058
NM_002693.3(POLG):c.2890C>T (p.Arg964Cys)	rs201477273	0.00033
NM_198994.3(TGM6):c.1550T>G (p.Leu517Trp)	rs387907097	0.00006

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