List of variants in gene F8 reported as benign by Invitae

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.4500G>A (p.Pro1500=)	rs33921347	0.01389
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.3621C>T (p.His1207=)	rs28370212	0.00371
NM_000132.4(F8):c.389-9C>T	rs35621875	0.00356
NM_000132.4(F8):c.2947G>A (p.Val983Ile)	rs35295375	0.00205
NM_000132.4(F8):c.102C>T (p.Asp34=)	rs1800283	0.00070
NM_000132.4(F8):c.5430T>G (p.Ser1810=)	rs142177821	0.00050
NM_000132.4(F8):c.1272-5T>C	rs377416503	0.00016

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