List of variants reported as benign for hematologic disorder by Clingen Thrombosis Variant Curation Expert Panel, ClinGen

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000488.4(SERPINC1):c.1011A>G (p.Gln337=)	rs5878	0.48194
NM_000488.4(SERPINC1):c.981A>G (p.Val327=)	rs5877	0.48114
NM_000488.4(SERPINC1):c.1154-53G>A	rs2759328	0.09559
NM_000488.4(SERPINC1):c.1218+27G>C	rs677	0.09086
NM_000488.4(SERPINC1):c.42-18C>T	rs2227599	0.02503
NM_000488.4(SERPINC1):c.914C>A (p.Pro305His)	rs549991084	0.00001

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