Variants with conflicting interpretations "benign" from Northcott Neuroscience Laboratory, ANZAC Research Institute and "likely benign" from Genome Diagnostics Laboratory, University Medical Center Utrecht

Minimum review status of the submission from Northcott Neuroscience Laboratory, ANZAC Research Institute:		Collection method of the submission from Northcott Neuroscience Laboratory, ANZAC Research Institute:
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_015046.7(SETX):c.7640T>C (p.Ile2547Thr)	rs151117904	0.00431
NM_001605.3(AARS1):c.2185C>T (p.Arg729Trp)	rs138081804	0.00072

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