Variants with conflicting interpretations "pathogenic" from Clingen Thrombosis Variant Curation Expert Panel, ClinGen and "likely pathogenic" from Labcorp Genetics (formerly Invitae), Labcorp

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000488.4(SERPINC1):c.1157T>C (p.Ile386Thr)	rs1449772752
NM_000488.4(SERPINC1):c.1277C>T (p.Ser426Leu)	rs121909550

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