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 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.070 1.000 7 2005 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.070 1.000 7 2005 2018
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.020 1.000 2 2005 2018
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.020 1.000 2 2005 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.020 1.000 2 2005 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.020 1.000 2 2005 2019
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2005 2005
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2005 2005
Malignant neoplasm of urinary bladder
316 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2005 2005
Xeroderma Pigmentosum, Complementation Group D
111 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2005 2005
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.030 1.000 3 2006 2014
Malignant neoplasm of colon and/or rectum
502 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.030 1.000 3 2006 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2006 2006
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.020 1.000 2 2007 2010
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2007 2007
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2007 2007
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2007 2007
Biliary Tract Cancer
CUI: C0750952
Disease: Biliary Tract Cancer
11 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2008 2008
Familial multiple trichoepitheliomata
32 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2008 2008
Glioma
CUI: C0017638
Disease: Glioma
353 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 0.040 1.000 4 2009 2018