rs4149584
|
0.683 |
0.440 |
12 |
6333477 |
missense variant |
C/G;T
|
snv
|
4.0E-06;
1.3E-02
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.900 |
0.933 |
15 |
1999 |
2019 |
rs1800693
|
0.776 |
0.360 |
12 |
6330843 |
non coding transcript exon variant |
T/C
|
snv
|
0.36;
4.0E-06
|
0.38
|
Multiple Sclerosis
|
Immune System Diseases; Nervous System Diseases
|
0.880 |
1.000 |
12 |
2009 |
2019 |
rs104895218
|
0.827 |
0.240 |
12 |
6334099 |
missense variant |
C/T
|
snv
|
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.850 |
1.000 |
9 |
1999 |
2014 |
rs104895219
|
0.827 |
0.240 |
12 |
6333823 |
missense variant |
G/A;T
|
snv
|
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.840 |
1.000 |
12 |
1999 |
2019 |
rs104895221
|
0.925 |
0.200 |
12 |
6333490 |
missense variant |
A/G
|
snv
|
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.810 |
1.000 |
6 |
1999 |
2008 |
rs104895222
|
1.000 |
0.120 |
12 |
6333489 |
missense variant |
C/T
|
snv
|
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.810 |
1.000 |
6 |
1999 |
2010 |
rs104895228
|
0.925 |
0.120 |
12 |
6333764 |
missense variant |
A/C;G;T
|
snv
|
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.810 |
1.000 |
6 |
1999 |
2014 |
rs104895217
|
1.000 |
0.120 |
12 |
6334109 |
missense variant |
A/G
|
snv
|
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
5 |
1999 |
2004 |
rs104895220
|
1.000 |
0.120 |
12 |
6333817 |
missense variant |
C/A;T
|
snv
|
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
5 |
1999 |
2004 |
rs104895223
|
0.882 |
0.240 |
12 |
6334108 |
missense variant |
C/A;G;T
|
snv
|
4.0E-06
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
5 |
1999 |
2004 |
rs104895225
|
1.000 |
0.120 |
12 |
6334100 |
missense variant |
A/C
|
snv
|
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
5 |
1999 |
2004 |
rs1800693
|
0.776 |
0.360 |
12 |
6330843 |
non coding transcript exon variant |
T/C
|
snv
|
0.36;
4.0E-06
|
0.38
|
Primary biliary cirrhosis
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
0.800 |
1.000 |
3 |
2011 |
2015 |
rs4149637
|
0.851 |
0.320 |
12 |
6333835 |
missense variant |
G/A;C
|
snv
|
5.7E-03
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.710 |
1.000 |
6 |
1999 |
2005 |
rs104895271
|
0.851 |
0.240 |
12 |
6334161 |
missense variant |
A/C;G
|
snv
|
1.6E-04;
4.8E-05
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
6 |
2006 |
2014 |
rs104895254
|
1.000 |
0.120 |
12 |
6334131 |
missense variant |
G/C
|
snv
|
|
|
TNF receptor-associated periodic fever syndrome (TRAPS)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
5 |
1999 |
2004 |
rs1860545
|
0.790 |
0.200 |
12 |
6337611 |
intron variant |
G/A
|
snv
|
|
0.31
|
Ankylosing spondylitis
|
Musculoskeletal Diseases
|
0.700 |
1.000 |
2 |
2013 |
2016 |
rs4149581
|
1.000 |
0.080 |
12 |
6337819 |
intron variant |
T/A;C
|
snv
|
|
|
Primary biliary cirrhosis
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
0.700 |
1.000 |
2 |
2011 |
2012 |
rs1800692
|
0.925 |
0.120 |
12 |
6333180 |
missense variant |
A/G
|
snv
|
0.64
|
0.71
|
Eosinophil count procedure
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs1800693
|
0.776 |
0.360 |
12 |
6330843 |
non coding transcript exon variant |
T/C
|
snv
|
0.36;
4.0E-06
|
0.38
|
Biliary cirrhosis
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1860545
|
0.790 |
0.200 |
12 |
6337611 |
intron variant |
G/A
|
snv
|
|
0.31
|
Psoriasis
|
Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1860545
|
0.790 |
0.200 |
12 |
6337611 |
intron variant |
G/A
|
snv
|
|
0.31
|
Primary biliary cirrhosis
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs1860545
|
0.790 |
0.200 |
12 |
6337611 |
intron variant |
G/A
|
snv
|
|
0.31
|
Ulcerative Colitis
|
Digestive System Diseases
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1860545
|
0.790 |
0.200 |
12 |
6337611 |
intron variant |
G/A
|
snv
|
|
0.31
|
Cholangitis, Sclerosing
|
Digestive System Diseases
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1860545
|
0.790 |
0.200 |
12 |
6337611 |
intron variant |
G/A
|
snv
|
|
0.31
|
Crohn Disease
|
Digestive System Diseases
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs2284344
|
|
|
12 |
6336163 |
intron variant |
G/C
|
snv
|
|
0.49
|
Platelet Count measurement
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |