List of variants studied for blood coagulation disease by Clinical Genomics Laboratory, Washington University in St. Louis

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000361.3(THBD):c.127G>A (p.Ala43Thr)	rs1800576	0.00255
NM_000204.5(CFI):c.1642G>C (p.Glu548Gln)	rs7437875	0.00206
NM_139027.6(ADAMTS13):c.3178C>T (p.Arg1060Trp)	rs142572218	0.00088
NM_000128.4(F11):c.901T>C (p.Phe301Leu)	rs121965064	0.00065
NM_003647.3(DGKE):c.235C>G (p.Gln79Glu)	rs143468147	0.00046
NM_139027.6(ADAMTS13):c.2936G>A (p.Arg979Gln)	rs142779872	0.00041
NM_000064.4(C3):c.1645G>A (p.Asp549Asn)
NM_000186.4(CFH):c.3152C>T (p.Pro1051Leu)
NM_000186.4(CFH):c.3565C>T (p.Leu1189Phe)	rs2149118712
NM_000361.3(THBD):c.670T>G (p.Cys224Gly)
NM_139027.6(ADAMTS13):c.2011C>T (p.Pro671Ser)
NM_139027.6(ADAMTS13):c.4039G>A (p.Gly1347Ser)
NM_139027.6(ADAMTS13):c.58G>A (p.Ala20Thr)
NM_139027.6(ADAMTS13):c.965G>T (p.Cys322Phe)

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