Variants with conflicting interpretations "likely pathogenic" from Laboratory of Medical Genetics, University of Torino and "pathogenic" from OMIM

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_003073.5(SMARCB1):c.110G>A (p.Arg37His)	rs398122368
NM_017780.4(CHD7):c.3082A>G (p.Ile1028Val)	rs121434338
NM_170675.5(MEIS2):c.992GAA[2] (p.Arg333del)	rs879255264

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