Variants with conflicting interpretations "likely pathogenic" from UCLA Clinical Genomics Center, UCLA and "pathogenic" from Genome-Nilou Lab

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004004.6(GJB2):c.109G>A (p.Val37Ile)	rs72474224	0.00354
NM_000402.4(G6PD):c.653C>T (p.Ser218Phe)	rs5030868	0.00028
NM_001042492.3(NF1):c.7909C>T (p.Arg2637Ter)	rs786201367
NM_022455.5(NSD1):c.5304-1G>C	rs863224905

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