Variants with conflicting interpretations "likely pathogenic" from Department of Vascular Biology, Beijing Anzhen Hospital and "uncertain significance" from Ambry Genetics

Minimum review status of the submission from Department of Vascular Biology, Beijing Anzhen Hospital:		Collection method of the submission from Department of Vascular Biology, Beijing Anzhen Hospital:
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_000138.5(FBN1):c.7540G>A (p.Gly2514Arg)	rs363811

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