Variants with conflicting interpretations "pathogenic" from Unidad de Estudios Geneticos y Forenses, Instituto Venezolano de Investigaciones Cientificas and "uncertain significance" from any submitter

Minimum review status of the submission from Unidad de Estudios Geneticos y Forenses, Instituto Venezolano de Investigaciones Cientificas:		Collection method of the submission from Unidad de Estudios Geneticos y Forenses, Instituto Venezolano de Investigaciones Cientificas:
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_000492.4(CFTR):c.1117G>A (p.Asp373Asn)	rs556880586	0.00003

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