Variants with conflicting interpretations "pathogenic" from Laboratory of Neurogenetics and Neuroinflammation, Institut Imagine and "likely pathogenic" 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.*686A>G	rs201558321	0.00006
NM_022168.4(IFIH1):c.2336G>T (p.Arg779Leu)	rs587777446
NM_183065.4(TMEM107):c.*696A>G	rs779456932
NM_183065.4(TMEM107):c.*745C>G	rs746503581

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