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.
Childhood Hodgkin Lymphoma
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
29 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2011 2011
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
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
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
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
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2011 2011
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
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
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
Meningioma
CUI: C0025286
Disease: Meningioma
43 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2010 2010
Meningioma, benign, no ICD-O subtype
30 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2010 2010
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2011 2011
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
Xeroderma Pigmentosum, Complementation Group D
111 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2006 2006