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: rs5743312
rs5743312 		0.827 0.160 4 186079102 intron variant C/T snv 0.14
CUI: C0206139
Disease: Lichen Planus, Oral
Lichen Planus, Oral 		Skin and Connective Tissue Diseases; Stomatognathic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs5743312
rs5743312 		0.827 0.160 4 186079102 intron variant C/T snv 0.14
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs5743312
rs5743312 		0.827 0.160 4 186079102 intron variant C/T snv 0.14
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs5743312
rs5743312 		0.827 0.160 4 186079102 intron variant C/T snv 0.14
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs5743312
rs5743312 		0.827 0.160 4 186079102 intron variant C/T snv 0.14
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs5743312
rs5743312 		0.827 0.160 4 186079102 intron variant C/T snv 0.14
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs5743313
rs5743313 		0.851 0.200 4 186079213 intron variant C/T snv 0.19
CUI: C0155870
Disease: Pneumonia and influenza
Pneumonia and influenza 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5743313
rs5743313 		0.851 0.200 4 186079213 intron variant C/T snv 0.19
CUI: C0032285
Disease: Pneumonia
Pneumonia 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5743313
rs5743313 		0.851 0.200 4 186079213 intron variant C/T snv 0.19
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs5743313
rs5743313 		0.851 0.200 4 186079213 intron variant C/T snv 0.19
CUI: C3825816
Disease: Pneumonia in children
Pneumonia in children 		0.010 1.000 1 2012 2012
dbSNP: rs5743314
rs5743314 		0.851 0.160 4 186079221 intron variant G/C;T snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2017 2017
dbSNP: rs5743314
rs5743314 		0.851 0.160 4 186079221 intron variant G/C;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs5743314
rs5743314 		0.851 0.160 4 186079221 intron variant G/C;T snv
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017
dbSNP: rs5743314
rs5743314 		0.851 0.160 4 186079221 intron variant G/C;T snv
CUI: C0023895
Disease: Liver diseases
Liver diseases 		Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs5743314
rs5743314 		0.851 0.160 4 186079221 intron variant G/C;T snv
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs5743315
rs5743315 		1.000 0.080 4 186079262 intron variant C/A;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2012 2012
dbSNP: rs7657186
rs7657186 		4 186072885 intron variant G/A snv 0.21
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 < 0.001 1 2014 2014
dbSNP: rs7657186
rs7657186 		4 186072885 intron variant G/A snv 0.21
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 < 0.001 1 2014 2014
dbSNP: rs7668666
rs7668666 		1.000 4 186080138 intron variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 < 0.001 1 2014 2014
dbSNP: rs7668666
rs7668666 		1.000 4 186080138 intron variant C/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 < 0.001 1 2014 2014
dbSNP: rs7668666
rs7668666 		1.000 4 186080138 intron variant C/A;T snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs7668666
rs7668666 		1.000 4 186080138 intron variant C/A;T snv
CUI: C0677944
Disease: Sentinel node (disorder)
Sentinel node (disorder) 		0.010 1.000 1 2013 2013
dbSNP: rs78726532
rs78726532 		1.000 0.080 4 186079310 intron variant A/G snv 4.0E-02
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2017 2017
dbSNP: rs1554064929
rs1554064929 		1.000 4 186083922 stop gained G/T snv
CUI: C2751803
Disease: HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 2
HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 2 		0.700 0
dbSNP: rs776400293
rs776400293 		4 186076620 start lost A/G snv 4.0E-06 7.0E-06
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2015 2015