List of variants in gene F8 reported as benign by ClinGen Coagulation Factor Deficiency Variant Curation Expert Panel, Clingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.3864A>C (p.Ser1288=)	rs1800292	0.09246
NM_000132.4(F8):c.6769A>G (p.Met2257Val)	rs1800297	0.07378
NM_000132.4(F8):c.1086G>A (p.Ala362=)	rs1800289	0.01123
NM_000132.4(F8):c.1508G>A (p.Arg503His)	rs35383156	0.00563
NM_000132.4(F8):c.2947G>A (p.Val983Ile)	rs35295375	0.00205
NM_000132.4(F8):c.2453C>T (p.Thr818Ile)	rs142274278	0.00080
NM_000132.4(F8):c.6724G>A (p.Val2242Met)	rs782654096	0.00008
NM_000132.4(F8):c.3280G>A (p.Glu1094Lys)	rs377119670
NM_000132.4(F8):c.5703C>A (p.Ile1901=)	rs782721473

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