Variants with conflicting interpretations "likely benign" from Clingen Thrombosis Variant Curation Expert Panel, ClinGen and "uncertain significance" 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000488.4(SERPINC1):c.-57G>A	rs372524963	0.00029
NM_000488.4(SERPINC1):c.29C>A (p.Thr10Asn)	rs61736655	0.00029
NM_000488.4(SERPINC1):c.870C>T (p.Phe290=)	rs370190321	0.00026
NM_000488.4(SERPINC1):c.299A>G (p.Asp100Gly)	rs369524182	0.00008
NM_000488.4(SERPINC1):c.47T>C (p.Val16Ala)	rs531137446	0.00008
NM_000488.4(SERPINC1):c.594T>C (p.Tyr198=)	rs183416252	0.00005
NM_000488.4(SERPINC1):c.408+4C>T	rs201551398	0.00001
NM_000488.4(SERPINC1):c.21A>T (p.Gly7=)	rs2526612908

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