Source: BEFREE

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: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.060 1.000 6 2009 2017
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.060 1.000 6 2009 2017
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.050 1.000 5 2007 2013
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.040 1.000 4 2011 2018
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.030 1.000 3 2011 2018
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.030 0.667 3 2010 2017
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
Malignant neoplasm of colon and/or rectum
0.020 1.000 2 2007 2018
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 1.000 2 2007 2018
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 1.000 2 2009 2011
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 1.000 2 2014 2015
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.020 1.000 2 2009 2018
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 0.500 2 2014 2015
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.020 1.000 2 2009 2018
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.010 1.000 1 2016 2016
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.010 1.000 1 2013 2013
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
0.010 1.000 1 2011 2011
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2007 2007
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma
0.010 1.000 1 2009 2009
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection
0.010 1.000 1 2018 2018
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.010 < 0.001 1 2016 2016
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0019693
Disease: HIV Infections
HIV Infections
0.010 1.000 1 2019 2019
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C4722518
Disease: Triple-Negative Breast Carcinoma
Triple-Negative Breast Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0751571
Disease: Cancer of Urinary Tract
Cancer of Urinary Tract
0.010 1.000 1 2016 2016
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial
0.010 1.000 1 2009 2009
dbSNP: rs1801157
rs1801157
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2018 2018