Variants with conflicting interpretations "pathogenic" from Laboratory of Neurogenetics and Neuroinflammation, Institut Imagine and "uncertain significance" from any submitter

Minimum review status of the submission from Laboratory of Neurogenetics and Neuroinflammation, Institut Imagine:		Collection method of the submission from Laboratory of Neurogenetics and Neuroinflammation, Institut Imagine:
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: 4

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HGVS	dbSNP	gnomAD frequency
NM_183065.4(TMEM107):c.*617C>T	rs117735243
NM_183065.4(TMEM107):c.*634C>T	rs545394298
NM_183065.4(TMEM107):c.*718G>A	rs201686383
NM_183065.4(TMEM107):c.*745C>G	rs746503581

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