Variants with conflicting interpretations "uncertain significance" from Biomedical Genomics and Oncogenetics Laboratory, Institut Pasteur de Tunis, University Tunis El Manar and "pathogenic" from any submitter

Minimum review status of the submission from Biomedical Genomics and Oncogenetics Laboratory, Institut Pasteur de Tunis, University Tunis El Manar:		Collection method of the submission from Biomedical Genomics and Oncogenetics Laboratory, Institut Pasteur de Tunis, University Tunis El Manar:
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_017547.4(FOXRED1):c.1261G>A (p.Val421Met)	rs199542988	0.00004
NM_032380.5(GFM2):c.569G>A (p.Arg190Gln)	rs761283105	0.00003

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