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: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.100 0.900 20 1998 2017
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.100 0.900 20 1998 2017
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.100 0.900 20 1998 2017
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.090 1.000 9 2012 2018
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.090 1.000 9 2012 2018
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.090 1.000 9 2012 2018
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.080 1.000 8 2001 2016
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.080 1.000 8 2001 2016
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.070 1.000 7 2008 2017
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
Malignant neoplasm of colon and/or rectum
0.060 1.000 6 2008 2017
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.060 1.000 6 2003 2019
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.050 1.000 5 2003 2019
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.050 1.000 5 2005 2019
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.050 1.000 5 2005 2019
dbSNP: rs4646903
rs4646903
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.050 1.000 5 2011 2017
dbSNP: rs4646903
rs4646903
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.050 1.000 5 2011 2017
dbSNP: rs4646903
rs4646903
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.050 1.000 5 2011 2017
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0235782
Disease: Gallbladder Carcinoma
Gallbladder Carcinoma
0.040 0.500 4 2007 2014
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.040 1.000 4 2005 2014
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
0.040 1.000 4 2008 2016
dbSNP: rs4646903
rs4646903
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.040 0.750 4 2010 2016
dbSNP: rs4646903
rs4646903
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.040 0.750 4 2010 2016
dbSNP: rs4646903
rs4646903
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.040 1.000 4 2010 2017
dbSNP: rs4646903
rs4646903
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 0.750 4 2016 2018
dbSNP: rs4646903
rs4646903
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.040 0.750 4 2010 2016