Variants with conflicting interpretations "uncertain significance" from Baylor Genetics and "likely benign" from University of Washington Department of Laboratory Medicine, University of Washington

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.394G>A (p.Val132Ile)	rs201141245	0.00007
NM_000535.7(PMS2):c.632G>A (p.Arg211Gln)	rs587781934	0.00006
NM_032043.3(BRIP1):c.689C>T (p.Ser230Leu)	rs759031349	0.00006

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