FGA and venous thromboembolism: Our reference panel shows an insertion of 28 bp at chr4:154584089 (dbSNP: rs148317511; ClinVar: RCV000247066) in a high linkage (phased r = 0.98) with rs6050-C, a missense mutation in FGA associated with venous thromboembolism [50– 53] and chronic thromboembolic pulmonary hypertension [53, 54].