Variants with conflicting interpretations "uncertain significance" from Baylor Genetics and "likely benign" 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_021098.3(CACNA1H):c.2626G>A (p.Ala876Thr)	rs58173258	0.00169
NM_000466.3(PEX1):c.3373A>T (p.Met1125Leu)	rs142994610	0.00065
NM_016180.5(SLC45A2):c.1518C>T (p.Val506=)	rs150473213	0.00034

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