CD14, CD14 molecule, 929

N. diseases: 551; N. variants: 8
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: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0155877
Disease: Allergic asthma
Allergic asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		Digestive System Diseases; Infections 0.010 1.000 1 2009 2009
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.010 1.000 1 2005 2005
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization 		0.010 1.000 1 2010 2010
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.010 1.000 1 2013 2013
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0277528
Disease: Traveler's diarrhea
Traveler's diarrhea 		Digestive System Diseases; Infections 0.010 1.000 1 2011 2011
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2020 2020
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C4554344
Disease: IgE-mediated food allergy
IgE-mediated food allergy 		Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2020 2020
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2014 2014
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0035243
Disease: Respiratory Tract Infections
Respiratory Tract Infections 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C4520983
Disease: Congenital atresia of extrahepatic bile duct
Congenital atresia of extrahepatic bile duct 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs5744455
rs5744455 		0.882 0.160 5 140633722 upstream gene variant G/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2020 2020
dbSNP: rs5744455
rs5744455 		0.882 0.160 5 140633722 upstream gene variant G/A;T snv
CUI: C0595989
Disease: Carcinoma of larynx
Carcinoma of larynx 		Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs5744455
rs5744455 		0.882 0.160 5 140633722 upstream gene variant G/A;T snv
CUI: C0007107
Disease: Malignant neoplasm of larynx
Malignant neoplasm of larynx 		Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs5744455
rs5744455 		0.882 0.160 5 140633722 upstream gene variant G/A;T snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs5744455
rs5744455 		0.882 0.160 5 140633722 upstream gene variant G/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2020 2020