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

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.575C>A (p.Ser192Tyr)	rs1042602	0.24593
NM_000287.4(PEX6):c.1802G>A (p.Arg601Gln)	rs34324426	0.00294
NM_000275.3(OCA2):c.1320G>C (p.Leu440Phe)	rs1800408	0.00024
NM_000098.3(CPT2):c.691C>T (p.Arg231Trp)	rs373638740	0.00004

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