rs5743836, TLR9

N. diseases: 31
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.
Meningococcal meningitis
CUI: C0025294
Disease: Meningococcal meningitis
3 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2017 2017
Adult Burkitt Lymphoma
CUI: C0278764
Disease: Adult Burkitt Lymphoma
7 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2012 2012
Childhood Burkitt Lymphoma
CUI: C0278879
Disease: Childhood Burkitt Lymphoma
7 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2012 2012
Chronic gastritis
CUI: C0085695
Disease: Chronic gastritis
11 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2019 2019
Burkitt Lymphoma
CUI: C0006413
Disease: Burkitt Lymphoma
13 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2012 2012
Community acquired pneumonia
CUI: C0694549
Disease: Community acquired pneumonia
13 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2016 2016
Cancer of Digestive System
CUI: C0751075
Disease: Cancer of Digestive System
15 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2014 2014
Meningitis, Bacterial
CUI: C0085437
Disease: Meningitis, Bacterial
16 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1 2016 2016
Latent Tuberculosis
CUI: C1609538
Disease: Latent Tuberculosis
18 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2015 2015
Spondylarthritis
CUI: C0949690
Disease: Spondylarthritis
23 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2019 2019
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2012 2012
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2012 2012
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2013 2013
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2017 2017
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2011 2011
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2012 2012
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2018 2018
HIV Infections
CUI: C0019693
Disease: HIV Infections
142 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2017 2017
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2018 2018
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2012 2012
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2019 2019
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2017 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2009 2009
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.020 1.000 2 2009 2011
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.050 0.600 5 2007 2017