Table 1.

Description of the selected single-nucleotide polymorphisms (SNPs)

Hemostatic risk allele	Approved name	Approved symbol	HGNC ID	Chromosomal location	RS	Point mutation nucleotide	Allele type
Beta-Fibrinogen 455 G/A	Fibrinogen beta chain	FGB	3662	4q31.3	rs1800790	455	G/A
GpIIb/IIIa PIA2	Integrin subunit beta 3	ITGB3	6156	17q21.32	rs5918	1565	T/C
Factor V Leiden	Coagulation factor V	F5	3542	1q24.2	rs6025	506	G/A
Factor VH2R	Coagulation factor V	F5	3542	1q24.2	rs1800595	1299	T/C
Prothrombin G20210A	Coagulation factor II, thrombin	F2	3535	11p11.2	rs1799963	20,210	G/A

A, adenine; C, cytosine; G, guanine; GpIIIa, glycoprotein IIIa; HGNC, HUGO Gene Nomenclature Committee; RS, reference sequence; T, thymine