Variants with conflicting interpretations "uncertain significance" from UOSD Laboratory of Genetics & Genomics of Rare Diseases, Istituto Giannina Gaslini and "likely benign" from Invitae

Minimum review status of the submission from UOSD Laboratory of Genetics & Genomics of Rare Diseases, Istituto Giannina Gaslini:		Collection method of the submission from UOSD Laboratory of Genetics & Genomics of Rare Diseases, Istituto Giannina Gaslini:
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: 1

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HGVS	dbSNP	gnomAD frequency
NM_017491.5(WDR1):c.1433C>T (p.Thr478Met)	rs186889066	0.00080

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