rs3138053, NFKBIA

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Adult Hodgkin Lymphoma
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
27 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2015 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2015 2015
Childhood Hodgkin Lymphoma
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
29 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2015 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2013 2013
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2015 2015
Invasive Streptococcus pneumoniae disease
CUI: C1320214
Disease: Invasive Streptococcus pneumoniae disease
9 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2007 2007
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2015 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2015 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2015 2015
SVEINSSON CHORIORETINAL ATROPHY
CUI: C1862382
Disease: SVEINSSON CHORIORETINAL ATROPHY
30 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2014 2014