rs587776742
|
1.000 |
0.120 |
X |
48683854 |
start lost |
A/T
|
snv
|
|
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs587776745
|
1.000 |
0.120 |
X |
48683860 |
frameshift variant |
G/-
|
delins
|
|
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs193922415
|
1.000 |
0.120 |
X |
48683890 |
stop gained |
C/T
|
snv
|
|
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1557006239
|
0.882 |
0.120 |
X |
48683944 |
missense variant |
G/A
|
snv
|
|
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
10 |
1995 |
2017 |
rs1557006239
|
0.882 |
0.120 |
X |
48683944 |
missense variant |
G/A
|
snv
|
|
|
THROMBOCYTOPENIA 1 (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
10 |
1995 |
2017 |
rs1557006239
|
0.882 |
0.120 |
X |
48683944 |
missense variant |
G/A
|
snv
|
|
|
Neutropenia, Severe Congenital, X-Linked
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
10 |
1995 |
2017 |
rs132630271
|
1.000 |
0.120 |
X |
48683953 |
stop gained |
C/A;T
|
snv
|
5.5E-06
|
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs132630273
|
0.925 |
0.120 |
X |
48684284 |
missense variant |
C/T
|
snv
|
|
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
12 |
1995 |
2010 |
rs132630273
|
0.925 |
0.120 |
X |
48684284 |
missense variant |
C/T
|
snv
|
|
|
THROMBOCYTOPENIA 1 (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.810 |
1.000 |
6 |
1995 |
2017 |
rs132630273
|
0.925 |
0.120 |
X |
48684284 |
missense variant |
C/T
|
snv
|
|
|
Thrombocytopenia
|
Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs132630269
|
1.000 |
0.080 |
X |
48684317 |
missense variant |
C/T
|
snv
|
|
|
THROMBOCYTOPENIA 1 (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs132630275
|
0.925 |
0.080 |
X |
48684323 |
missense variant |
C/A;G
|
snv
|
|
|
THROMBOCYTOPENIA 1 (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
5 |
1995 |
2002 |
rs132630275
|
0.925 |
0.080 |
X |
48684323 |
missense variant |
C/A;G
|
snv
|
|
|
Thrombocytopenia, X-Linked, Intermittent
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs782290433
|
0.882 |
0.120 |
X |
48684373 |
missense variant |
G/A
|
snv
|
5.5E-06
|
|
THROMBOCYTOPENIA 1 (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
17 |
1995 |
2017 |
rs782290433
|
0.882 |
0.120 |
X |
48684373 |
missense variant |
G/A
|
snv
|
5.5E-06
|
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
13 |
1995 |
2017 |
rs782290433
|
0.882 |
0.120 |
X |
48684373 |
missense variant |
G/A
|
snv
|
5.5E-06
|
|
Neutropenia, Severe Congenital, X-Linked
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
13 |
1995 |
2017 |
rs132630272
|
0.925 |
0.120 |
X |
48684394 |
missense variant |
T/C
|
snv
|
|
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
12 |
1995 |
2010 |
rs132630272
|
0.925 |
0.120 |
X |
48684394 |
missense variant |
T/C
|
snv
|
|
|
WISKOTT-ALDRICH SYNDROME, ATTENUATED
|
|
0.700 |
|
0 |
|
|
rs132630268
|
0.882 |
0.120 |
X |
48684407 |
missense variant |
G/A;C;T
|
snv
|
|
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.710 |
1.000 |
19 |
1994 |
2013 |
rs132630268
|
0.882 |
0.120 |
X |
48684407 |
missense variant |
G/A;C;T
|
snv
|
|
|
THROMBOCYTOPENIA 1 (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
9 |
1997 |
2013 |
rs132630268
|
0.882 |
0.120 |
X |
48684407 |
missense variant |
G/A;C;T
|
snv
|
|
|
Neutropenia, Severe Congenital, X-Linked
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
9 |
1997 |
2013 |
rs139857045
|
1.000 |
0.120 |
X |
48684416 |
missense variant |
G/A
|
snv
|
5.2E-05
|
1.1E-04
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
12 |
1995 |
2010 |
rs1557006354
|
0.882 |
0.120 |
X |
48684421 |
stop gained |
C/T
|
snv
|
|
|
THROMBOCYTOPENIA 1 (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1557006354
|
0.882 |
0.120 |
X |
48684421 |
stop gained |
C/T
|
snv
|
|
|
Wiskott-Aldrich Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1557006354
|
0.882 |
0.120 |
X |
48684421 |
stop gained |
C/T
|
snv
|
|
|
Neutropenia, Severe Congenital, X-Linked
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|