Variants with conflicting interpretations "likely pathogenic" from Human Genetics Section, Sidra Medicine and "pathogenic" from any submitter

Minimum review status of the submission from Human Genetics Section, Sidra Medicine:		Collection method of the submission from Human Genetics Section, Sidra Medicine:
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_000138.5(FBN1):c.5087A>G (p.Tyr1696Cys)	rs387906625
NM_000685.5(AGTR1):c.415C>T (p.Arg139Ter)	rs1417391173
NM_003742.4(ABCB11):c.1789dup (p.Val597fs)
NM_014140.4(SMARCAL1):c.886del (p.Thr296fs)

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