Variants with conflicting interpretations "pathogenic" from Biomedical Innovation Departament, CIEMAT and "likely pathogenic" from Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum review status of the submission from Biomedical Innovation Departament, CIEMAT:		Collection method of the submission from Biomedical Innovation Departament, CIEMAT:
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_000213.5(ITGB4):c.2783-2A>G	rs758551913

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