IL32, interleukin 32, 9235

N. diseases: 200; N. variants: 6
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: rs4786370
rs4786370 		0.882 0.280 16 3063897 upstream gene variant T/C snv 0.42
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.020 1.000 2 2017 2018
dbSNP: rs12934561
rs12934561 		0.882 0.080 16 3068864 intron variant T/C snv 0.57
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs12934561
rs12934561 		0.882 0.080 16 3068864 intron variant T/C snv 0.57
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2015 2015
dbSNP: rs12934561
rs12934561 		0.882 0.080 16 3068864 intron variant T/C snv 0.57
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2015 2015
dbSNP: rs2015620
rs2015620 		0.882 0.120 16 3073560 intron variant A/G;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2015620
rs2015620 		0.882 0.120 16 3073560 intron variant A/G;T snv
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
Infection caused by Helicobacter pylori 		Infections 0.010 1.000 1 2016 2016
dbSNP: rs2015620
rs2015620 		0.882 0.120 16 3073560 intron variant A/G;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs28372698
rs28372698 		0.807 0.200 16 3065110 upstream gene variant T/A;C snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs28372698
rs28372698 		0.807 0.200 16 3065110 upstream gene variant T/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs28372698
rs28372698 		0.807 0.200 16 3065110 upstream gene variant T/A;C snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs28372698
rs28372698 		0.807 0.200 16 3065110 upstream gene variant T/A;C snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs28372698
rs28372698 		0.807 0.200 16 3065110 upstream gene variant T/A;C snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs28372698
rs28372698 		0.807 0.200 16 3065110 upstream gene variant T/A;C snv
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2015 2015
dbSNP: rs28372698
rs28372698 		0.807 0.200 16 3065110 upstream gene variant T/A;C snv
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2015 2015
dbSNP: rs4349147
rs4349147 		16 3074919 intron variant A/G snv 0.69
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4786370
rs4786370 		0.882 0.280 16 3063897 upstream gene variant T/C snv 0.42
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4786370
rs4786370 		0.882 0.280 16 3063897 upstream gene variant T/C snv 0.42
CUI: C0002893
Disease: Refractory anemias
Refractory anemias 		Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9927163
rs9927163 		1.000 0.120 16 3066185 intron variant T/A;G snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2019 2019