rs34536443, TYK2

N. diseases: 25
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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.830 0.857 7 2012 2019
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.810 1.000 2 2012 2018
Oligoarticular Juvenile Idiopathic Arthritis
35 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.800 1.000 1 2013 2013
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.800 1.000 1 2012 2012
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.750 0.833 6 2013 2019
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.730 1.000 4 2015 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.730 1.000 4 2010 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2019 2019
Diabetes Mellitus, Insulin-Dependent
954 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2015 2015
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2019 2019
Juvenile pauciarticular chronic arthritis
31 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2013 2013
Juvenile-Onset Still Disease
CUI: C0087031
Disease: Juvenile-Onset Still Disease
41 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2013 2013
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2016 2016
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
31 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2013 2013
Psoriasis vulgaris
CUI: C0263361
Disease: Psoriasis vulgaris
80 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2015 2015
Rheumatoid Arthritis, Systemic Juvenile
42 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2013 2013
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2015 2015
Systemic onset juvenile chronic arthritis
53 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.700 1.000 1 2013 2013
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
89 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.010 1.000 1 2017 2017
Encephalitis, St. Louis
CUI: C0014060
Disease: Encephalitis, St. Louis
34 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.010 1.000 1 2019 2019
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.010 1.000 1 2015 2015
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.010 1.000 1 2017 2017
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.010 1.000 1 2018 2018