Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.060 1.000 6 2014 2019
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.060 1.000 6 2014 2019
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.060 0.833 6 2012 2018
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.050 0.800 5 2012 2018
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.050 0.800 5 2013 2019
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.040 1.000 4 2015 2019
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.040 1.000 4 2015 2019
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.040 1.000 4 2015 2019
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0023895
Disease: Liver diseases
Liver diseases
Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
Malignant neoplasm of gastrointestinal tract
Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 < 0.001 1 2014 2014
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2018 2018
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C1333015
Disease: Childhood Kidney Wilms Tumor
Childhood Kidney Wilms Tumor
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2018 2018
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2014 2014
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs6505162
rs6505162
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013