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: rs5744454
rs5744454 		1.000 0.040 5 140633982 upstream gene variant T/C;G snv
CUI: C2747816
Disease: Complicated malaria
Complicated malaria 		Infections 0.010 1.000 1 2018 2018
dbSNP: rs2569191
rs2569191 		1.000 0.080 5 140634318 upstream gene variant C/A;T snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2569191
rs2569191 		1.000 0.080 5 140634318 upstream gene variant C/A;T snv
CUI: C0043144
Disease: Wheezing
Wheezing 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs2569192
rs2569192 		0.925 0.120 5 140635623 upstream gene variant G/C snv 0.27
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2569192
rs2569192 		0.925 0.120 5 140635623 upstream gene variant G/C snv 0.27
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2915863
rs2915863 		0.925 0.160 5 140634792 upstream gene variant C/A;T snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2915863
rs2915863 		0.925 0.160 5 140634792 upstream gene variant C/A;T snv
CUI: C0043144
Disease: Wheezing
Wheezing 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs2915863
rs2915863 		0.925 0.160 5 140634792 upstream gene variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4914
rs4914 		0.925 0.160 5 140631883 synonymous variant C/A;G snv 4.8E-05; 9.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs4914
rs4914 		0.925 0.160 5 140631883 synonymous variant C/A;G snv 4.8E-05; 9.3E-02
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: 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
dbSNP: rs2563298
rs2563298 		0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2014 2014
dbSNP: rs2563298
rs2563298 		0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2014 2014
dbSNP: rs2563298
rs2563298 		0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2563298
rs2563298 		0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System 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: C0031099
Disease: Periodontitis
Periodontitis 		Stomatognathic Diseases 0.030 0.667 3 2016 2019
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.020 1.000 2 2014 2015
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.020 1.000 2 2014 2015
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 1.000 2 2011 2012
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.020 1.000 2 2009 2019
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma 		Immune System Diseases 0.010 1.000 1 2015 2015