Variants with conflicting interpretations "pathogenic" from UCLA Clinical Genomics Center, UCLA and "uncertain significance" from any submitter

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_001065.4(TNFRSF1A):c.362G>A (p.Arg121Gln)	rs4149584	0.01206
NM_000435.3(NOTCH3):c.3691C>T (p.Arg1231Cys)	rs201680145	0.00089

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