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: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.020 1.000 2 2013 2019
dbSNP: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0019693
Disease: HIV Infections
HIV Infections
Infections; Immune System Diseases 0.020 1.000 2 2014 2019
dbSNP: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.020 1.000 2 2013 2019
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: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections
Infections 0.020 0.500 2 2016 2017
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: rs352140
rs352140
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49
CUI: C0085437
Disease: Meningitis, Bacterial
Meningitis, Bacterial
Infections; Nervous System Diseases 0.020 1.000 2 2016 2017
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: 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: rs1475539937
rs1475539937
0.882 0.120 3 52223085 missense variant A/G snv 4.0E-06
CUI: C0004623
Disease: Bacterial Infections
Bacterial Infections
Infections 0.010 1.000 1 2012 2012
dbSNP: rs1475539937
rs1475539937
0.882 0.120 3 52223085 missense variant A/G snv 4.0E-06
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1475539937
rs1475539937
0.882 0.120 3 52223085 missense variant A/G snv 4.0E-06
CUI: C0857069
Disease: Chronic candidiasis
Chronic candidiasis
Infections 0.010 1.000 1 2012 2012
dbSNP: rs1475539937
rs1475539937
0.882 0.120 3 52223085 missense variant A/G snv 4.0E-06
CUI: C0006846
Disease: Cutaneous Candidiasis
Cutaneous Candidiasis
Infections; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
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
dbSNP: rs187084
rs187084
0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs187084
rs187084
0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C1855179
Disease: CATARACT, ANTERIOR POLAR
CATARACT, ANTERIOR POLAR
Eye Diseases 0.010 1.000 1 2016 2016
dbSNP: rs187084
rs187084
0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis
Infections; Respiratory Tract Diseases 0.010 1.000 1 2016 2016