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: 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
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		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: C0751075
Disease: Cancer of Digestive System
Cancer of Digestive System 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs187084
rs187084 		0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0043144
Disease: Wheezing
Wheezing 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2016 2016
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: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System 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: 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: C0263746
Disease: Osteoarthritis of the hand
Osteoarthritis of the hand 		Musculoskeletal 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: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive 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: 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