rs121918151
|
1.000 |
0.080 |
2 |
127428426 |
missense variant |
C/T
|
snv
|
|
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
7 |
1992 |
2015 |
rs121918144
|
1.000 |
0.080 |
2 |
127428462 |
missense variant |
C/T
|
snv
|
|
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs121918147
|
1.000 |
0.080 |
2 |
127428587 |
missense variant |
G/A
|
snv
|
4.0E-06
|
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs121918157
|
1.000 |
0.080 |
2 |
127428895 |
missense variant |
C/G
|
snv
|
4.0E-06
|
7.0E-06
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1254257945
|
1.000 |
0.080 |
2 |
127423405 |
missense variant |
G/A;C
|
snv
|
6.8E-06;
4.1E-05
|
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs121918150
|
0.925 |
0.080 |
2 |
127428560 |
missense variant |
G/A;T
|
snv
|
8.0E-06
|
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
7 |
1992 |
2015 |
rs121918148
|
0.925 |
0.080 |
2 |
127421397 |
missense variant |
A/C
|
snv
|
|
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs767730328
|
0.925 |
0.080 |
2 |
127428660 |
missense variant |
T/C
|
snv
|
4.0E-06
|
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs121918143
|
0.882 |
0.080 |
2 |
127426180 |
missense variant |
C/A;T
|
snv
|
4.0E-06;
2.8E-05
|
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs121918149
|
0.882 |
0.080 |
2 |
127421438 |
missense variant |
G/A
|
snv
|
5.2E-05
|
7.7E-05
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs121918156
|
0.882 |
0.120 |
2 |
127427219 |
missense variant |
C/T
|
snv
|
|
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs121918146
|
0.827 |
0.200 |
2 |
127428485 |
missense variant |
G/A
|
snv
|
1.2E-05
|
2.1E-05
|
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|