NFKBIA, NFKB inhibitor alpha, 4792

N. diseases: 226; N. variants: 19
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: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2016 2016
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0028960
Disease: Oligospermia
Oligospermia 		Male Urogenital Diseases 0.010 1.000 1 2016 2016
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2018 2018
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2016 2016
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
Adult Hodgkin Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs696
rs696 		0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 < 0.001 1 2016 2016
dbSNP: rs2233406
rs2233406 		0.732 0.440 14 35405593 upstream gene variant G/A snv 0.26
CUI: C1862382
Disease: SVEINSSON CHORIORETINAL ATROPHY
SVEINSSON CHORIORETINAL ATROPHY 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2233406
rs2233406 		0.732 0.440 14 35405593 upstream gene variant G/A snv 0.26
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs2233406
rs2233406 		0.732 0.440 14 35405593 upstream gene variant G/A snv 0.26
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2015 2015