Source: ALL

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: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 1.000 2 2011 2013
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.020 1.000 2 2015 2016
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
Malignant neoplasm of gallbladder
0.020 1.000 2 2009 2011
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.020 1.000 2 2012 2015
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C0235782
Disease: Gallbladder Carcinoma
Gallbladder Carcinoma
0.020 1.000 2 2009 2011
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.020 1.000 2 2009 2014
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
Stage IIA Gallbladder Cancer AJCC v8
0.020 1.000 2 2009 2011
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 1.000 2 2009 2013
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.020 1.000 2 2012 2015
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C4525297
Disease: Stage 0 Gallbladder Cancer AJCC v8
Stage 0 Gallbladder Cancer AJCC v8
0.020 1.000 2 2009 2011
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 1.000 2 2009 2014
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.020 0.500 2 2006 2009
dbSNP: rs2066826
rs2066826
0.851 0.160 1 186676795 intron variant C/T snv 0.14 0.19
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.020 1.000 2 2010 2015
dbSNP: rs2066826
rs2066826
0.851 0.160 1 186676795 intron variant C/T snv 0.14 0.19
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.020 1.000 2 2010 2015
dbSNP: rs2066826
rs2066826
0.851 0.160 1 186676795 intron variant C/T snv 0.14 0.19
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.020 1.000 2 2010 2015
dbSNP: rs5275
rs5275
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.020 1.000 2 2012 2018
dbSNP: rs5275
rs5275
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 0.500 2 2008 2011
dbSNP: rs5275
rs5275
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 0.500 2 2008 2011
dbSNP: rs5275
rs5275
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.020 1.000 2 2012 2018
dbSNP: rs5275
rs5275
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 1.000 2 2013 2013
dbSNP: rs5275
rs5275
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.020 1.000 2 2012 2018
dbSNP: rs5275
rs5275
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 1.000 2 2011 2013
dbSNP: rs5277
rs5277
0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06
CUI: C0030193
Disease: Pain
Pain
0.020 1.000 2 2012 2015
dbSNP: rs689466
rs689466
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17
Squamous cell carcinoma of the head and neck
0.020 0.500 2 2015 2016
dbSNP: rs689466
rs689466
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 1.000 2 2011 2016