List of variants reported as pathogenic for blood coagulation disease by Reproductive Health Research and Development, BGI Genomics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.2561G>A (p.Arg854Gln)	rs41276738	0.00377
NM_000301.5(PLG):c.112A>G (p.Lys38Glu)	rs73015965	0.00282
NM_000128.4(F11):c.403G>T (p.Glu135Ter)	rs121965063	0.00066
NM_000128.4(F11):c.901T>C (p.Phe301Leu)	rs121965064	0.00065
NM_001001548.3(CD36):c.268C>T (p.Pro90Ser)	rs75326924	0.00011
NM_001001548.3(CD36):c.332_333del (p.Thr111fs)	rs572295823

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