List of variants reported as likely benign by Clingen Thrombosis Variant Curation Expert Panel, ClinGen

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000488.4(SERPINC1):c.529C>T (p.Arg177Cys)	rs143521873	0.00041
NM_000488.4(SERPINC1):c.29C>A (p.Thr10Asn)	rs61736655	0.00029
NM_000488.4(SERPINC1):c.1154-5T>C	rs375346550	0.00005
NM_000488.4(SERPINC1):c.1254C>T (p.Thr418=)	rs559277597	0.00003
NM_000488.4(SERPINC1):c.408+4C>T	rs201551398	0.00001
NM_000488.4(SERPINC1):c.881G>A (p.Arg294His)	rs587776397	0.00001
NM_000488.4(SERPINC1):c.1350C>T (p.Asn450=)
NM_000488.4(SERPINC1):c.51T>C (p.Tyr17=)	rs2102790373
NM_000488.4(SERPINC1):c.553A>G (p.Thr185Ala)	rs574547491

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