List of variants reported as likely benign for blood coagulation disease by Mendelics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.3980A>G (p.His1327Arg)	rs1800595	0.05074
NM_000204.5(CFI):c.1534+5G>T	rs114013791	0.00951
NM_001754.5(RUNX1):c.*4188G>C	rs761390141	0.00010
NM_000132.4(F8):c.6429+8606G>C	rs1603432445

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