rs121909551
|
1.000 |
0.080 |
1 |
173914743 |
missense variant |
G/A
|
snv
|
8.2E-04
|
9.0E-04
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
27 |
1986 |
2019 |
rs121909552
|
0.925 |
0.080 |
1 |
173914725 |
missense variant |
C/T
|
snv
|
9.5E-05
|
1.7E-04
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
26 |
1984 |
2017 |
rs121909546
|
1.000 |
0.080 |
1 |
173903978 |
missense variant |
C/T
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
23 |
1986 |
2013 |
rs121909547
|
1.000 |
0.080 |
1 |
173914726 |
missense variant |
G/A;T
|
snv
|
4.8E-05
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
22 |
1986 |
2019 |
rs121909548
|
1.000 |
0.080 |
1 |
173904038 |
missense variant |
C/A;G
|
snv
|
8.9E-04
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909549
|
1.000 |
0.080 |
1 |
173904010 |
missense variant |
C/G;T
|
snv
|
4.0E-06
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909550
|
1.000 |
0.080 |
1 |
173904007 |
missense variant |
G/A;C
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909554
|
1.000 |
0.080 |
1 |
173904011 |
missense variant |
G/A
|
snv
|
4.0E-06
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909555
|
1.000 |
0.080 |
1 |
173903968 |
missense variant |
G/A
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909557
|
1.000 |
0.080 |
1 |
173904044 |
missense variant |
C/T
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909558
|
1.000 |
0.080 |
1 |
173914845 |
missense variant |
A/T
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909564
|
1.000 |
0.080 |
1 |
173903902 |
missense variant |
G/A
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909565
|
1.000 |
0.080 |
1 |
173909564 |
missense variant |
A/G
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909566
|
1.000 |
0.080 |
1 |
173904013 |
missense variant |
C/T
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909567
|
0.925 |
0.120 |
1 |
173914570 |
missense variant |
G/A
|
snv
|
1.6E-05
|
7.0E-06
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2019 |
rs121909569
|
1.000 |
0.080 |
1 |
173911981 |
missense variant |
A/G
|
snv
|
1.2E-05
|
1.4E-05
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909571
|
1.000 |
0.080 |
1 |
173910861 |
missense variant |
T/C
|
snv
|
4.0E-06
|
1.4E-05
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909572
|
1.000 |
0.080 |
1 |
173910849 |
missense variant |
A/G
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909573
|
1.000 |
0.080 |
1 |
173914582 |
missense variant |
A/G
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs387906575
|
1.000 |
0.080 |
1 |
173914893 |
missense variant |
A/G
|
snv
|
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
21 |
1986 |
2013 |
rs121909563
|
1.000 |
0.080 |
1 |
173911941 |
missense variant |
C/A;T
|
snv
|
1.6E-05;
4.0E-06
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
20 |
1986 |
2013 |
rs28929469
|
1.000 |
0.080 |
1 |
173914795 |
missense variant |
G/A
|
snv
|
2.0E-05
|
7.0E-06
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
|
0 |
|
|
rs2227624
|
1.000 |
0.080 |
1 |
173914872 |
missense variant |
A/T
|
snv
|
1.8E-03
|
1.7E-03
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.710 |
1.000 |
1 |
2016 |
2016 |
rs1170430756
|
1.000 |
0.080 |
1 |
173911987 |
missense variant |
T/C
|
snv
|
8.0E-06
|
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
20 |
1986 |
2013 |
rs121909568
|
1.000 |
0.080 |
1 |
173904028 |
missense variant |
G/A
|
snv
|
4.0E-06
|
7.0E-06
|
Antithrombin III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
20 |
1986 |
2013 |