Variants with conflicting interpretations "uncertain significance" from Clingen Thrombosis Variant Curation Expert Panel, ClinGen and "likely pathogenic" from any submitter

Minimum review status of the submission from Clingen Thrombosis Variant Curation Expert Panel, ClinGen:		Collection method of the submission from Clingen Thrombosis Variant Curation Expert Panel, ClinGen:
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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000488.4(SERPINC1):c.1141T>C (p.Ser381Pro)	rs121909565
NM_000488.4(SERPINC1):c.1247dup (p.Ser417fs)	rs2526543302
NM_000488.4(SERPINC1):c.1376C>A (p.Ala459Asp)	rs1572084448
NM_000488.4(SERPINC1):c.1393T>C (p.Ter465Gln)	rs1572084425
NM_000488.4(SERPINC1):c.536T>C (p.Phe179Ser)	rs483352847
NM_000488.4(SERPINC1):c.592T>C (p.Tyr198His)	rs1572090114

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