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: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.060 1.000 6 2011 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.060 1.000 6 2011 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.040 1.000 4 2017 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.040 1.000 4 2017 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2017 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.020 1.000 2 2015 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.020 1.000 2 2015 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma 		0.020 0.500 2 2018 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		0.020 1.000 2 2018 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.020 1.000 2 2015 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
Liver and Intrahepatic Biliary Tract Carcinoma 		0.020 0.500 2 2018 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver 		0.020 0.500 2 2018 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.020 1.000 2 2017 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		0.010 1.000 1 2015 2015
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0007104
Disease: Female Breast Carcinoma
Female Breast Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 < 0.001 1 2018 2018
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2019 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2019 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0235653
Disease: Malignant neoplasm of female breast
Malignant neoplasm of female breast 		0.010 1.000 1 2017 2017
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2019 2019
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 < 0.001 1 2018 2018
dbSNP: rs3787016
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 < 0.001 1 2018 2018