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.
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
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
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
Asthma
CUI: C0004096
Disease: Asthma
1536 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1 2011 2011
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
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
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
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
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
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
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
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.020 1.000 2 2013 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.020 1.000 2 2013 2014
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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2014 2014
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2014 2014
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
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
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.658 0.440 3 52226766 intron variant A/G snv 0.20 0.010 1.000 1 2016 2016
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
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
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
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