TSLP, thymic stromal lymphopoietin, 85480

N. diseases: 220; N. variants: 9
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: rs3806932
rs3806932 		0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.720 1.000 3 2011 2016
dbSNP: rs3806932
rs3806932 		0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases 0.720 1.000 2 2010 2015
dbSNP: rs1898671
rs1898671 		0.851 0.160 5 111072304 intron variant C/T snv 0.25
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.710 1.000 2 2011 2019
dbSNP: rs10455025
rs10455025 		1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs10455025
rs10455025 		1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10455025
rs10455025 		1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1898671
rs1898671 		0.851 0.160 5 111072304 intron variant C/T snv 0.25
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1898671
rs1898671 		0.851 0.160 5 111072304 intron variant C/T snv 0.25
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		0.700 1.000 1 2019 2019
dbSNP: rs2289277
rs2289277 		1.000 0.080 5 111073369 5 prime UTR variant C/A;G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs3806932
rs3806932 		0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs3806933
rs3806933 		0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs3806933
rs3806933 		0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2289276
rs2289276 		0.882 0.160 5 111071809 5 prime UTR variant C/T snv 0.27
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.030 1.000 3 2010 2014
dbSNP: rs3806933
rs3806933 		0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 1.000 2 2011 2014
dbSNP: rs10062929
rs10062929 		1.000 0.120 5 111072481 intron variant C/A snv 0.13
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs11466749
rs11466749 		0.925 0.120 5 111076887 3 prime UTR variant A/G snv 0.15
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs11466749
rs11466749 		0.925 0.120 5 111076887 3 prime UTR variant A/G snv 0.15
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1898671
rs1898671 		0.851 0.160 5 111072304 intron variant C/T snv 0.25
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1898671
rs1898671 		0.851 0.160 5 111072304 intron variant C/T snv 0.25
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2289276
rs2289276 		0.882 0.160 5 111071809 5 prime UTR variant C/T snv 0.27
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2289276
rs2289276 		0.882 0.160 5 111071809 5 prime UTR variant C/T snv 0.27
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2289277
rs2289277 		1.000 0.080 5 111073369 5 prime UTR variant C/A;G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2289277
rs2289277 		1.000 0.080 5 111073369 5 prime UTR variant C/A;G;T snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2289278
rs2289278 		0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2289278
rs2289278 		0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016