Variants with conflicting interpretations "uncertain significance" from Laboratory of Medical Genetics, University of Torino and "likely pathogenic" from any submitter

Minimum review status of the submission from Laboratory of Medical Genetics, University of Torino:		Collection method of the submission from Laboratory of Medical Genetics, University of Torino:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001375524.1(TRRAP):c.5713A>G (p.Lys1905Glu)	rs1791437854
NM_020822.3(KCNT1):c.108del (p.Arg37fs)
NM_201599.3(ZMYM3):c.1322G>A (p.Arg441Gln)

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