Variants with conflicting interpretations "likely benign" from Research Unit of Translational Medicine, University of Oulu and "uncertain significance" from any submitter

Minimum review status of the submission from Research Unit of Translational Medicine, University of Oulu:		Collection method of the submission from Research Unit of Translational Medicine, University of Oulu:
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_007194.4(CHEK2):c.1312G>T (p.Asp438Tyr)	rs200050883	0.00034

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