TLR3, toll like receptor 3, 7098

N. diseases: 393; N. variants: 24
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: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.020 1.000 2 2011 2016
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.020 1.000 2 2016 2019
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.020 1.000 2 2011 2016
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2015 2019
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.020 1.000 2 2011 2016
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 1.000 2 2015 2016
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0085437
Disease: Meningitis, Bacterial
Meningitis, Bacterial 		Infections; Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		Musculoskeletal Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections 		Infections 0.010 1.000 1 2017 2017
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs3775290
rs3775290 		0.742 0.280 4 186083063 missense variant C/A;T snv 0.30
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		Digestive System Diseases; Infections 0.010 1.000 1 2016 2016
dbSNP: rs3775291
rs3775291 		0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.070 1.000 7 2009 2016
dbSNP: rs3775291
rs3775291 		0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.060 0.667 6 2008 2018
dbSNP: rs3775291
rs3775291 		0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy 		Eye Diseases 0.030 1.000 3 2008 2016
dbSNP: rs3775291
rs3775291 		0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.020 1.000 2 2014 2016
dbSNP: rs3775291
rs3775291 		0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		Digestive System Diseases; Infections 0.020 1.000 2 2013 2018
dbSNP: rs3775291
rs3775291 		0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C0014061
Disease: Tick-Borne Encephalitis
Tick-Borne Encephalitis 		Infections; Nervous System Diseases 0.020 1.000 2 2013 2017
dbSNP: rs3775291
rs3775291 		0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.020 1.000 2 2013 2018
dbSNP: rs3775291
rs3775291 		0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3775291
rs3775291 		0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3775291
rs3775291 		0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C0019345
Disease: Herpes Labialis
Herpes Labialis 		Infections; Skin and Connective Tissue Diseases; Stomatognathic Diseases 0.010 1.000 1 2012 2012