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: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.050 1.000 5 2012 2019
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.050 0.400 5 2012 2016
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.050 1.000 5 2012 2019
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.050 1.000 5 2012 2019
dbSNP: rs5743836
rs5743836 		0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.050 0.600 5 2007 2017
dbSNP: rs352139
rs352139 		0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.040 0.500 4 2012 2017
dbSNP: rs352139
rs352139 		0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.040 1.000 4 2012 2015
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.030 1.000 3 2013 2019
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		Infections; Respiratory Tract Diseases 0.030 1.000 3 2014 2018
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.030 1.000 3 2013 2019
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: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.020 1.000 2 2012 2019
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: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		Infections; Respiratory Tract Diseases 0.020 1.000 2 2015 2019
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: rs5743836
rs5743836 		0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.020 1.000 2 2009 2011
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2017 2017
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2010 2010
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: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2011 2011
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0019158
Disease: Hepatitis
Hepatitis 		Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2017 2017