Variants with conflicting interpretations "likely pathogenic" from Center for Medical Genetics, GenVams Trust and "pathogenic" from any submitter

Minimum review status of the submission from Center for Medical Genetics, GenVams Trust:		Collection method of the submission from Center for Medical Genetics, GenVams Trust:
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_000211.5(ITGB2):c.322C>T (p.Arg108Ter)	rs772471533

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