Variants with conflicting interpretations "likely pathogenic" from Intergen, Intergen Genetics and Rare Diseases Diagnosis Center and "uncertain significance" from any submitter

Minimum review status of the submission from Intergen, Intergen Genetics and Rare Diseases Diagnosis Center:		Collection method of the submission from Intergen, Intergen Genetics and Rare Diseases Diagnosis Center:
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_000065.5(C6):c.2381+2T>C	rs76202909	0.00242

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