List of variants in gene F8 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.2947G>A (p.Val983Ile)	rs35295375	0.00205
NM_000132.4(F8):c.4333T>C (p.Ser1445Pro)	rs146153504	0.00129
NM_000132.4(F8):c.5430T>G (p.Ser1810=)	rs142177821	0.00050
NM_000132.4(F8):c.6115+27C>T	rs375609267	0.00039
NM_000132.4(F8):c.1064G>A (p.Arg355Gln)	rs146581224	0.00019
NM_000132.4(F8):c.6276G>A (p.Val2092=)	rs199522131	0.00019
NM_000132.4(F8):c.2887G>A (p.Asp963Asn)	rs199660138	0.00017
NM_000132.4(F8):c.3399A>G (p.Gly1133=)	rs200042130	0.00015
NM_000132.4(F8):c.5604A>T (p.Ser1868=)	rs782028903	0.00006
NM_000132.4(F8):c.3376A>T (p.Arg1126Trp)	rs199630813	0.00004
NM_000132.4(F8):c.144-13T>G	rs782248521	0.00001
NM_000132.4(F8):c.2961G>C (p.Glu987Asp)
NM_000132.4(F8):c.312C>A (p.Val104=)

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