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: rs13126816
rs13126816 		0.925 0.200 4 186073024 intron variant G/A snv 0.21
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: rs13126816
rs13126816 		0.925 0.200 4 186073024 intron variant G/A snv 0.21
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.020 1.000 2 2013 2015
dbSNP: rs5743305
rs5743305 		0.807 0.200 4 186068179 upstream gene variant T/A snv 0.35
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.020 1.000 2 2009 2016
dbSNP: rs11721827
rs11721827 		0.851 0.200 4 186069983 intron variant A/C snv 0.12
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs11721827
rs11721827 		0.851 0.200 4 186069983 intron variant A/C snv 0.12
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs11721827
rs11721827 		0.851 0.200 4 186069983 intron variant A/C snv 0.12
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: rs11721827
rs11721827 		0.851 0.200 4 186069983 intron variant A/C snv 0.12
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs1879026
rs1879026 		1.000 0.080 4 186079167 intron variant G/C;T snv
CUI: C0023895
Disease: Liver diseases
Liver diseases 		Digestive System Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs1879026
rs1879026 		1.000 0.080 4 186079167 intron variant G/C;T snv
CUI: C0019158
Disease: Hepatitis
Hepatitis 		Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1879026
rs1879026 		1.000 0.080 4 186079167 intron variant G/C;T snv
CUI: C0019159
Disease: Hepatitis A
Hepatitis A 		Digestive System Diseases; Infections 0.010 1.000 1 2018 2018
dbSNP: rs3775292
rs3775292 		0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs3775292
rs3775292 		0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs3775292
rs3775292 		0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82
CUI: C0677944
Disease: Sentinel node (disorder)
Sentinel node (disorder) 		0.010 1.000 1 2013 2013
dbSNP: rs3775292
rs3775292 		0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs3775292
rs3775292 		0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs5743305
rs5743305 		0.807 0.200 4 186068179 upstream gene variant T/A snv 0.35
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs5743305
rs5743305 		0.807 0.200 4 186068179 upstream gene variant T/A snv 0.35
CUI: C0014061
Disease: Tick-Borne Encephalitis
Tick-Borne Encephalitis 		Infections; Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs5743305
rs5743305 		0.807 0.200 4 186068179 upstream gene variant T/A snv 0.35
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs5743305
rs5743305 		0.807 0.200 4 186068179 upstream gene variant T/A snv 0.35
CUI: C0018572
Disease: Hand, Foot and Mouth Disease
Hand, Foot and Mouth Disease 		Infections 0.010 1.000 1 2018 2018
dbSNP: rs5743305
rs5743305 		0.807 0.200 4 186068179 upstream gene variant T/A snv 0.35
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2018 2018
dbSNP: rs5743305
rs5743305 		0.807 0.200 4 186068179 upstream gene variant T/A snv 0.35
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs5743305
rs5743305 		0.807 0.200 4 186068179 upstream gene variant T/A snv 0.35
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: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff 		Nutritional and Metabolic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs5743312
rs5743312 		0.827 0.160 4 186079102 intron variant C/T snv 0.14
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		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: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014