rs61754966, NBN

N. diseases: 23
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.
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.720 1.000 2 2004 2014
Childhood Acute Lymphoblastic Leukemia
261 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.720 1.000 2 2013 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.070 0.857 7 2007 2013
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.060 0.833 6 2008 2015
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.060 0.833 6 2008 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.040 1.000 4 2007 2013
leukemia
CUI: C0023418
Disease: leukemia
144 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.030 1.000 3 2008 2013
Malignant neoplasm of larynx
CUI: C0007107
Disease: Malignant neoplasm of larynx
50 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.030 1.000 3 2007 2013
Adult Medulloblastoma
CUI: C0278876
Disease: Adult Medulloblastoma
24 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.020 1.000 2 2010 2011
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.020 1.000 2 2008 2013
Childhood Medulloblastoma
CUI: C0278510
Disease: Childhood Medulloblastoma
25 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.020 1.000 2 2010 2011
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.020 1.000 2 2008 2008
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
115 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.020 1.000 2 2010 2011
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.010 1.000 1 2004 2004
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.010 1.000 1 2008 2008
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.010 1.000 1 2013 2013
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.010 1.000 1 2008 2008
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.010 1.000 1 2014 2014
Hematologic Neoplasms
CUI: C0376545
Disease: Hematologic Neoplasms
60 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.010 1.000 1 2004 2004
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.010 1.000 1 2008 2008
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.010 1.000 1 2007 2007
Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.010 1.000 1 2004 2004
Solid Neoplasm
CUI: C0280100
Disease: Solid Neoplasm
24 0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 0.010 1.000 1 2011 2011