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: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs352140
rs352140 		0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0003467
Disease: Anxiety
Anxiety 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs5743836
rs5743836 		0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs352140
rs352140 		0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs352140
rs352140 		0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.010 1.000 1 2013 2013
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: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.020 1.000 2 2014 2014
dbSNP: rs352140
rs352140 		0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.020 1.000 2 2009 2019
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: 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: C0085695
Disease: Chronic gastritis
Chronic gastritis 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0023895
Disease: Liver diseases
Liver diseases 		Digestive System Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs352139
rs352139 		0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54
CUI: C0019158
Disease: Hepatitis
Hepatitis 		Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs352139
rs352139 		0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs352140
rs352140 		0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs352140
rs352140 		0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs352140
rs352140 		0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0019158
Disease: Hepatitis
Hepatitis 		Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs5743836
rs5743836 		0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0085695
Disease: Chronic gastritis
Chronic gastritis 		Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs5743836
rs5743836 		0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs5743836
rs5743836 		0.658 0.440 3 52226766 intron variant A/G snv 0.20
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs352140
rs352140 		0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.020 1.000 2 2014 2017
dbSNP: rs1475539937
rs1475539937 		0.882 0.120 3 52223085 missense variant A/G snv 4.0E-06
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2016 2016
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0019159
Disease: Hepatitis A
Hepatitis A 		Digestive System Diseases; Infections 0.010 1.000 1 2018 2018