Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.050 0.600 5 2007 2017
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2013 2014
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.020 1.000 2 2009 2011
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2013 2014
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		0.010 1.000 1 2018 2018
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0278764
Disease: Adult Burkitt Lymphoma
Adult Burkitt Lymphoma 		0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.010 1.000 1 2009 2009
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C1609538
Disease: Latent Tuberculosis
Latent Tuberculosis 		0.010 1.000 1 2015 2015
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2018 2018
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0025294
Disease: Meningococcal meningitis
Meningococcal meningitis 		0.010 1.000 1 2017 2017
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2019 2019
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma 		0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma 		0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0085437
Disease: Meningitis, Bacterial
Meningitis, Bacterial 		0.010 < 0.001 1 2016 2016
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		0.010 1.000 1 2011 2011
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0398623
Disease: Thrombophilia
Thrombophilia 		0.010 1.000 1 2017 2017
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0004096
Disease: Asthma
Asthma 		0.010 < 0.001 1 2011 2011
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0278879
Disease: Childhood Burkitt Lymphoma
Childhood Burkitt Lymphoma 		0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0019693
Disease: HIV Infections
HIV Infections 		0.010 1.000 1 2017 2017
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2014 2014
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0085695
Disease: Chronic gastritis
Chronic gastritis 		0.010 1.000 1 2019 2019
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0751075
Disease: Cancer of Digestive System
Cancer of Digestive System 		0.010 1.000 1 2014 2014
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0694549
Disease: Community acquired pneumonia
Community acquired pneumonia 		0.010 1.000 1 2016 2016
dbSNP: rs5743836
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection 		0.010 1.000 1 2013 2013