Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.100 0.878 49 2001 2019
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.100 0.878 49 2001 2019
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.100 0.921 38 2003 2019
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.100 0.921 38 2003 2019
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.100 0.921 38 2003 2019
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.100 0.960 25 2004 2017
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
Xeroderma Pigmentosum, Complementation Group D
0.100 0.960 25 2004 2016
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.833 24 2004 2016
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.100 0.842 19 2009 2020
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.100 0.750 16 2002 2018
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.100 0.750 16 2002 2018
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.813 16 2003 2018
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
Malignant neoplasm of colon and/or rectum
0.100 0.867 15 2004 2015
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0017638
Disease: Glioma
Glioma
0.100 0.933 15 2010 2017
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.100 0.800 15 2003 2017
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.100 0.615 13 2004 2016
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
Malignant neoplasm of urinary bladder
0.100 0.615 13 2004 2016
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.100 0.833 12 2005 2019
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.100 0.583 12 2004 2016
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.100 0.900 10 2004 2018
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.100 0.900 10 2004 2018
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
Childhood Acute Lymphoblastic Leukemia
0.100 1.000 10 2007 2015
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.090 0.778 9 2005 2019
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.090 0.778 9 2005 2019
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
0.070 0.571 7 2005 2014