Variants with conflicting interpretations "likely pathogenic" from UCLA Clinical Genomics Center, UCLA and "uncertain significance" from Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001103146.3(GIGYF2):c.2378C>T (p.Ala793Val)	rs748538823	0.00005
NM_000554.6(CRX):c.124G>A (p.Glu42Lys)	rs863224863

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