rs34767364, NBN

N. diseases: 20
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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.040 1.000 4 2004 2013
Nijmegen Breakage Syndrome
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
144 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.740 1.000 4 2006 2012
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.030 1.000 3 2004 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.030 1.000 3 2004 2014
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.020 1.000 2 2001 2006
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.020 1.000 2 2006 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.020 1.000 2 2004 2013
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2006 2006
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2006 2006
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2004 2004
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2004 2004
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2004 2004
Developmental delay (disorder)
CUI: C0424605
Disease: Developmental delay (disorder)
68 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2006 2006
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
553 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2006 2006
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2004 2004
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2004 2004
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2004 2004
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1 2006 2006
melanoma
CUI: C0025202
Disease: melanoma
515 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1.000 1 2004 2004
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 0.010 1 2006 2006