List of variants reported as risk factor for inherited thrombophilia by OMIM

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_021871.4(FGA):c.991A>G (p.Thr331Ala)	rs6050	0.29452
NM_004132.5(HABP2):c.1601G>A (p.Gly534Glu)	rs7080536	0.02322

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