IL9, interleukin 9, 3578

N. diseases: 291; N. variants: 4
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: rs1799962
rs1799962 		0.925 0.080 5 135896167 upstream gene variant T/C;G snv 7.2E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1799962
rs1799962 		0.925 0.080 5 135896167 upstream gene variant T/C;G snv 7.2E-02
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1799962
rs1799962 		0.925 0.080 5 135896167 upstream gene variant T/C;G snv 7.2E-02
CUI: C0375023
Disease: Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site 		0.010 1.000 1 2010 2010
dbSNP: rs1859430
rs1859430 		0.925 0.080 5 135894824 intron variant G/A snv 0.20
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1859430
rs1859430 		0.925 0.080 5 135894824 intron variant G/A snv 0.20
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2069885
rs2069885 		0.851 0.120 5 135892476 missense variant G/A;C snv 0.11
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2069885
rs2069885 		0.851 0.120 5 135892476 missense variant G/A;C snv 0.11
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2069885
rs2069885 		0.851 0.120 5 135892476 missense variant G/A;C snv 0.11
CUI: C0035235
Disease: Respiratory Syncytial Virus Infections
Respiratory Syncytial Virus Infections 		Infections 0.010 1.000 1 2010 2010
dbSNP: rs2069885
rs2069885 		0.851 0.120 5 135892476 missense variant G/A;C snv 0.11
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2069885
rs2069885 		0.851 0.120 5 135892476 missense variant G/A;C snv 0.11
CUI: C0375023
Disease: Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site 		0.010 1.000 1 2010 2010
dbSNP: rs31564
rs31564 		0.925 0.080 5 135894564 intron variant G/A;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs31564
rs31564 		0.925 0.080 5 135894564 intron variant G/A;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs31564
rs31564 		0.925 0.080 5 135894564 intron variant G/A;T snv
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013