rs1801516, ATM

N. diseases: 39
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.100 0.786 14 2003 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.100 0.786 14 2003 2019
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2004 2004
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.070 0.714 7 2005 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.060 0.667 6 2005 2018
bilateral breast cancer
CUI: C0281267
Disease: bilateral breast cancer
17 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.020 0.500 2 2005 2006
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
59 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2008 2008
Brain Tumor, Primary
CUI: C0750974
Disease: Brain Tumor, Primary
8 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2008 2008
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
39 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2008 2008
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
115 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2008 2008
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.030 1.000 3 2009 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2009 2009
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2009 2009
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2009 2009
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2009 2009
melanoma
CUI: C0025202
Disease: melanoma
515 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.810 1.000 3 2011 2017
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.020 1.000 2 2011 2015
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2012 2012
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2012 2012
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2012 2012
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2012 2012
Malignant neoplasm of urinary bladder
316 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2012 2012
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2012 2012
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2014 2014
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 0.010 1.000 1 2014 2014