Variants with conflicting interpretations "pathogenic" from Baylor Genetics and "uncertain significance" from PreventionGenetics, part of Exact Sciences

Minimum review status of the submission from Baylor Genetics:		Collection method of the submission from Baylor Genetics:
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_000372.5(TYR):c.575C>A (p.Ser192Tyr)	rs1042602	0.24046
NM_000287.4(PEX6):c.1802G>A (p.Arg601Gln)	rs34324426	0.00283
NM_000275.3(OCA2):c.1320G>C (p.Leu440Phe)	rs1800408	0.00023

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