TLR7, toll like receptor 7, 51284

N. diseases: 276; N. variants: 13
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: rs3853839
rs3853839 		0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.080 0.875 8 2010 2019
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.040 1.000 4 2008 2018
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.030 1.000 3 2009 2016
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.020 1.000 2 2014 2017
dbSNP: rs179009
rs179009 		0.925 0.160 X 12885361 intron variant A/G;T snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.020 1.000 2 2014 2014
dbSNP: rs3853839
rs3853839 		0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.020 1.000 2 2014 2018
dbSNP: rs1634323
rs1634323 		0.882 0.200 X 12870008 intron variant A/G snv 0.11
CUI: C0085166
Disease: Bacterial Vaginosis
Bacterial Vaginosis 		Female Urogenital Diseases and Pregnancy Complications; Infections 0.010 1.000 1 2016 2016
dbSNP: rs1634323
rs1634323 		0.882 0.200 X 12870008 intron variant A/G snv 0.11
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1634323
rs1634323 		0.882 0.200 X 12870008 intron variant A/G snv 0.11
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 < 0.001 1 2015 2015
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C1840264
Disease: IMMUNE SUPPRESSION
IMMUNE SUPPRESSION 		0.010 1.000 1 2009 2009
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C0019099
Disease: Hemorrhagic Fever, Crimean
Hemorrhagic Fever, Crimean 		Infections 0.010 1.000 1 2015 2015
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2018 2018
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C3811653
Disease: Experimental Organism Basal Cell Carcinoma
Experimental Organism Basal Cell Carcinoma 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		Hemic and Lymphatic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		Infections 0.010 1.000 1 2010 2010
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff 		Nutritional and Metabolic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs179008
rs179008 		0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2008 2008
dbSNP: rs179009
rs179009 		0.925 0.160 X 12885361 intron variant A/G;T snv
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs179010
rs179010 		0.882 0.200 X 12884766 intron variant T/C snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs179010
rs179010 		0.882 0.200 X 12884766 intron variant T/C snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs179010
rs179010 		0.882 0.200 X 12884766 intron variant T/C snv
CUI: C0008055
Disease: Chikungunya Fever
Chikungunya Fever 		Infections 0.010 1.000 1 2017 2017
dbSNP: rs179012
rs179012 		1.000 0.080 X 12883443 intron variant G/A snv 0.42
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2014 2014