rs1805794, NBN

N. diseases: 41
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.
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.020 1.000 2 2012 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.020 1.000 2 2012 2018
Malignant neoplasm of urinary bladder
316 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.020 1.000 2 2012 2014
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2012 2012
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2013 2013
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2013 2013
Cancer of Urinary Tract
CUI: C0751571
Disease: Cancer of Urinary Tract
11 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.020 1.000 2 2014 2014
Cancer of Digestive System
CUI: C0751075
Disease: Cancer of Digestive System
15 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2014 2014
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2015 2015
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2015 2015
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
23 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2015 2015
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2015 2015
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2015 2015
Glioma
CUI: C0017638
Disease: Glioma
353 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2016 2016
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2018 2018
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2018 2018