Variants with conflicting interpretations "likely pathogenic" from GeneDx and "uncertain significance" from Natera, Inc.

Minimum review status of the submission from GeneDx:		Collection method of the submission from GeneDx:
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003060.4(SLC22A5):c.728A>C (p.Tyr243Ser)	rs1321621475	0.00009
NM_003060.4(SLC22A5):c.131C>T (p.Ala44Val)	rs199689597	0.00003

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