Variants with conflicting interpretations "pathogenic" from Forensic Genetics Laboratory, Harris County Institute of Forensic Sciences and "uncertain significance" from Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

Minimum review status of the submission from Forensic Genetics Laboratory, Harris County Institute of Forensic Sciences:		Collection method of the submission from Forensic Genetics Laboratory, Harris County Institute of Forensic Sciences:
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_001040151.2(SCN3B):c.328G>A (p.Val110Ile)	rs147205617	0.00029
NM_000335.5(SCN5A):c.80G>A (p.Arg27His)	rs199473045	0.00017

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