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: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.100 0.727 11 2004 2016
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 0.900 10 2002 2016
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.090 0.889 9 2004 2014
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.090 0.889 9 2004 2014
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.090 0.889 9 2002 2017
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.090 0.667 9 2001 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
Diabetes Mellitus, Non-Insulin-Dependent
0.090 0.889 9 2000 2017
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.090 0.667 9 2001 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.090 0.667 9 2001 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis
0.090 0.889 9 1999 2020
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.080 0.750 8 2003 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.080 1.000 8 2006 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.080 1.000 8 2005 2013
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.080 1.000 8 2005 2013
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
Malignant neoplasm of urinary bladder
0.080 1.000 8 2005 2013
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.070 0.857 7 2012 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.070 0.714 7 2002 2017
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.070 1.000 7 2004 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
Precursor Cell Lymphoblastic Leukemia Lymphoma
0.070 1.000 7 2004 2015
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.070 0.857 7 2012 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.060 0.833 6 2012 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma
0.060 1.000 6 2007 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.060 0.833 6 2008 2015
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.060 0.833 6 2007 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.060 0.833 6 2012 2018