rs1057519328
|
1.000 |
0.200 |
16 |
3249592 |
missense variant |
G/C
|
snv
|
|
2.1E-05
|
Behcet Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs751454741
|
1.000 |
0.200 |
16 |
3254736 |
missense variant |
C/T
|
snv
|
4.0E-06
|
|
Behcet Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs755659290
|
1.000 |
0.200 |
16 |
3249480 |
missense variant |
T/C
|
snv
|
1.2E-05
|
1.4E-05
|
Behcet Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs3743930
|
0.611 |
0.720 |
16 |
3254626 |
missense variant |
C/G;T
|
snv
|
7.1E-02
|
|
Behcet Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
0.050 |
0.800 |
5 |
2000 |
2015 |
rs61752717
|
0.583 |
0.840 |
16 |
3243407 |
missense variant |
T/A;C
|
snv
|
2.8E-04
|
|
Behcet Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
0.040 |
1.000 |
4 |
2000 |
2015 |
rs28940579
|
0.732 |
0.440 |
16 |
3243310 |
missense variant |
A/G;T
|
snv
|
2.2E-03;
4.0E-06
|
|
Behcet Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
0.020 |
1.000 |
2 |
2000 |
2004 |
rs28940580
|
0.742 |
0.560 |
16 |
3243447 |
missense variant |
C/A;G;T
|
snv
|
1.0E-04;
8.0E-06
|
|
Behcet Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
0.020 |
1.000 |
2 |
2013 |
2015 |
rs104895083
|
0.925 |
0.200 |
16 |
3247166 |
missense variant |
G/C;T
|
snv
|
4.0E-05;
1.2E-05
|
|
Behcet Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs104895094
|
0.851 |
0.320 |
16 |
3243403 |
missense variant |
T/A;C
|
snv
|
8.0E-06;
5.2E-03
|
|
Behcet Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2006 |
2006 |