Variants with conflicting interpretations "likely pathogenic" from UCLA Clinical Genomics Center, UCLA and "uncertain significance" from Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn

Minimum review status of the submission from UCLA Clinical Genomics Center, UCLA:		Collection method of the submission from UCLA Clinical Genomics Center, UCLA:
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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001069.3(TUBB2A):c.872A>C (p.Gln291Pro)	rs863224939

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