TLR9, toll like receptor 9, 54106

N. diseases: 457; N. variants: 11
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0024530
Disease: Malaria
Malaria
Infections 0.010 1.000 1 2012 2012
dbSNP: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
Musculoskeletal Diseases 0.010 1.000 1 2012 2012
dbSNP: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0278879
Disease: Childhood Burkitt Lymphoma
Childhood Burkitt Lymphoma
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
Childhood Non-Hodgkin Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0278879
Disease: Childhood Burkitt Lymphoma
Childhood Burkitt Lymphoma
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0006413
Disease: Burkitt Lymphoma
Burkitt Lymphoma
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0278764
Disease: Adult Burkitt Lymphoma
Adult Burkitt Lymphoma
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5743836
rs5743836
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs352139
rs352139
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs5743836
rs5743836
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection
Infections 0.010 1.000 1 2013 2013
dbSNP: rs187084
rs187084
0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.020 1.000 2 2011 2014
dbSNP: rs352139
rs352139
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.020 1.000 2 2014 2014
dbSNP: rs352139
rs352139
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.020 1.000 2 2014 2014
dbSNP: rs5743836
rs5743836
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.020 1.000 2 2013 2014
dbSNP: rs5743836
rs5743836
0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.020 1.000 2 2013 2014
dbSNP: rs187084
rs187084
0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs187084
rs187084
0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0751075
Disease: Cancer of Digestive System
Cancer of Digestive System
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs187084
rs187084
0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs187084
rs187084
0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
dbSNP: rs187084
rs187084
0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2014 2014