rs4149584, TNFRSF1A

N. diseases: 24
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
TNF receptor-associated periodic fever syndrome (TRAPS)
33 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.900 0.933 15 1999 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.100 0.909 11 2007 2018
Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome
8 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.050 1.000 5 2007 2019
Autoinflammatory Syndrome
CUI: C3890737
Disease: Autoinflammatory Syndrome
7 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.030 1.000 3 2006 2013
Tumor necrosis factor receptor associated periodic syndrome [TRAPS]
2 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.030 1.000 3 2010 2019
Familial Mediterranean Fever
CUI: C0031069
Disease: Familial Mediterranean Fever
82 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.020 1.000 2 2008 2010
Periodic fever
CUI: C0015974
Disease: Periodic fever
5 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.020 1.000 2 2001 2011
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.020 0.500 2 2002 2007
Adenitis
CUI: C0001416
Disease: Adenitis
1 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2011 2011
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2010 2010
Arthralgia
CUI: C0003862
Disease: Arthralgia
27 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2007 2007
Autoinflammatory disease
CUI: C3267073
Disease: Autoinflammatory disease
10 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2011 2011
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2005 2005
Cardiac Tamponade
CUI: C0007177
Disease: Cardiac Tamponade
1 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2017 2017
Clinically isolated syndrome
CUI: C2921627
Disease: Clinically isolated syndrome
2 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2008 2008
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2005 2005
Demyelinating Diseases
CUI: C0011303
Disease: Demyelinating Diseases
5 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2011 2011
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2013 2013
Fever
CUI: C0015967
Disease: Fever
66 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2011 2011
Headache
CUI: C0018681
Disease: Headache
75 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2014 2014
Lymphadenitis
CUI: C0024205
Disease: Lymphadenitis
2 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2011 2011
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2004 2004
Pericarditis
CUI: C0031046
Disease: Pericarditis
6 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2017 2017
Polyarthritis
CUI: C0162323
Disease: Polyarthritis
9 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2007 2007