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.
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
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
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
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.040 0.750 4 2006 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.060 1.000 6 2005 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.080 0.625 8 2009 2019
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
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.030 1.000 3 2006 2012
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
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
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.080 0.625 8 2009 2019
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
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
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.040 0.750 4 2006 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.060 1.000 6 2005 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.050 0.600 5 2005 2019
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
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
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
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
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
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
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
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