List of variants reported as likely benign for hemophilia A by Illumina Laboratory Services, Illumina

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.1508G>A (p.Arg503His)	rs35383156	0.00563
NM_000132.4(F8):c.2994T>G (p.His998Gln)	rs149853218	0.00419
NM_000132.4(F8):c.389-9C>T	rs35621875	0.00356
NM_000132.4(F8):c.*1379A>G	rs36101366	0.00127
NM_000132.4(F8):c.102C>T (p.Asp34=)	rs1800283	0.00070
NM_000132.4(F8):c.*30G>A	rs376482768	0.00020
NM_000132.4(F8):c.1064G>A (p.Arg355Gln)	rs146581224	0.00019
NM_000132.4(F8):c.2383A>G (p.Arg795Gly)	rs2228152	0.00016
NM_000132.4(F8):c.2212T>G (p.Tyr738Asp)	rs201721215	0.00015
NM_000132.4(F8):c.3885C>G (p.Asn1295Lys)	rs201393905	0.00011
NM_000132.4(F8):c.2217G>A (p.Glu739=)	rs781850654	0.00005
NM_000132.4(F8):c.748A>G (p.Met250Val)	rs781943293	0.00005
NM_000132.4(F8):c.2535C>A (p.Asp845Glu)	rs200316756	0.00003
NM_000132.4(F8):c.3981G>A (p.Thr1327=)	rs374245599	0.00002
NM_000132.4(F8):c.6957G>A (p.Pro2319=)	rs200902529	0.00001
NM_000132.4(F8):c.*992A>G	rs782499043
NM_000132.4(F8):c.4679C>G (p.Pro1560Arg)	rs782791962

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