List of variants reported as uncertain significance for hemophilia A by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.4442T>C (p.Leu1481Pro)	rs1800294	0.00007
NM_000132.4(F8):c.6374G>C (p.Ser2125Thr)	rs782363141	0.00005
NM_000132.4(F8):c.6871A>G (p.Thr2291Ala)	rs139348729	0.00003
NM_000132.4(F8):c.2732A>G (p.Asp911Gly)	rs782671808	0.00001
NM_000132.4(F8):c.1312A>T (p.Ile438Phe)

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