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: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0206682
Disease: Follicular thyroid carcinoma
Follicular thyroid carcinoma
Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs10766196
rs10766196
0.925 0.120 11 14891585 5 prime UTR variant A/G snv 0.35
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs10766196
rs10766196
0.925 0.120 11 14891585 5 prime UTR variant A/G snv 0.35
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency
Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs10766197
rs10766197
0.807 0.240 11 14900334 upstream gene variant G/A;C snv
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.010 1.000 1 2016 2016
dbSNP: rs10766197
rs10766197
0.807 0.240 11 14900334 upstream gene variant G/A;C snv
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency
Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10766197
rs10766197
0.807 0.240 11 14900334 upstream gene variant G/A;C snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs10766197
rs10766197
0.807 0.240 11 14900334 upstream gene variant G/A;C snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs10766197
rs10766197
0.807 0.240 11 14900334 upstream gene variant G/A;C snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs10766197
rs10766197
0.807 0.240 11 14900334 upstream gene variant G/A;C snv
CUI: C0151332
Disease: Active tuberculosis
Active tuberculosis
Infections 0.010 1.000 1 2016 2016
dbSNP: rs1562902
rs1562902
0.925 0.120 11 14896670 upstream gene variant C/T snv 0.55
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
Digestive System Diseases; Infections 0.010 1.000 1 2019 2019
dbSNP: rs1562902
rs1562902
0.925 0.120 11 14896670 upstream gene variant C/T snv 0.55
CUI: C0085584
Disease: Encephalopathies
Encephalopathies
Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1562902
rs1562902
0.925 0.120 11 14896670 upstream gene variant C/T snv 0.55
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs1993116
rs1993116
0.827 0.200 11 14888688 intron variant A/G snv 0.65
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1993116
rs1993116
0.827 0.200 11 14888688 intron variant A/G snv 0.65
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement
0.700 1.000 1 2010 2010
dbSNP: rs1993116
rs1993116
0.827 0.200 11 14888688 intron variant A/G snv 0.65
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2019 2019