List of variants in gene SERPINC1 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000488.4(SERPINC1):c.89T>A (p.Val30Glu)	rs2227624	0.00171
NM_000488.4(SERPINC1):c.1246G>C (p.Ala416Pro)	rs121909548
NM_000488.4(SERPINC1):c.244G>T (p.Glu82Ter)	rs1557904209
NM_000488.4(SERPINC1):c.42-1G>C	rs1572092195

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