List of variants in gene F2 reported as likely pathogenic for blood coagulation disease

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000506.5(F2):c.1814_1815del (p.His605fs)	rs776618390	0.00001
NM_000506.5(F2):c.260A>G (p.Tyr87Cys)	rs1227147475	0.00001
NC_000011.9:g.(?_46746328)_(46748347_?)del
NM_000506.3(F2):c.1273C>T (p.Arg425Cys)	rs121918479
NM_000506.5(F2):c.1070A>G (p.Glu357Gly)	rs2134533215
NM_000506.5(F2):c.1094T>A (p.Val365Glu)	rs747234596
NM_000506.5(F2):c.118C>T (p.Arg40Trp)
NM_000506.5(F2):c.1270G>A (p.Val424Met)	rs1310397756
NM_000506.5(F2):c.1496G>A (p.Gly499Glu)	rs2134537035
NM_000506.5(F2):c.1621C>T (p.Arg541Trp)	rs886048338
NM_000506.5(F2):c.1741C>T (p.Arg581Cys)
NM_000506.5(F2):c.1745G>A (p.Trp582Ter)
NM_000506.5(F2):c.1750C>T (p.Gln584Ter)	rs1401703940
NM_000506.5(F2):c.317-1G>A
NM_000506.5(F2):c.422+1G>A
NM_000506.5(F2):c.995G>C (p.Gly332Ala)	rs2134532862

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