List of variants in gene F8 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.6951C>G (p.Asp2317Glu)	rs782799573	0.00008
NM_000132.4(F8):c.1748A>G (p.Asn583Ser)	rs782657516	0.00003
NM_000132.4(F8):c.3986G>A (p.Arg1329His)	rs782767347	0.00001
NM_000132.4(F8):c.1264G>C (p.Asp422His)	rs370737113
NM_000132.4(F8):c.1727A>T (p.Glu576Val)	rs2523942153
NM_000132.4(F8):c.2009TCT[2] (p.Phe672del)	rs1476178386
NM_000132.4(F8):c.6574+5G>A

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