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: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 < 0.001 1 2015 2015
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.010 < 0.001 1 2015 2015
dbSNP: rs20417
rs20417
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv
Squamous cell carcinoma of the head and neck
0.010 < 0.001 1 2016 2016
dbSNP: rs2206593
rs2206593
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 < 0.001 1 2015 2015
dbSNP: rs2206593
rs2206593
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 < 0.001 1 2015 2015
dbSNP: rs2745557
rs2745557
0.807 0.200 1 186680089 intron variant A/G snv 0.83
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 < 0.001 1 2009 2009
dbSNP: rs367650109
rs367650109
1.000 0.080 1 186675959 missense variant A/G snv 4.0E-06 2.1E-05
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis
0.010 < 0.001 1 2005 2005
dbSNP: rs5273
rs5273
0.827 0.080 1 186674636 missense variant A/C;G snv 4.0E-06; 7.6E-03 1.4E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 < 0.001 1 2013 2013
dbSNP: rs5273
rs5273
0.827 0.080 1 186674636 missense variant A/C;G snv 4.0E-06; 7.6E-03 1.4E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 < 0.001 1 2006 2006
dbSNP: rs5273
rs5273
0.827 0.080 1 186674636 missense variant A/C;G snv 4.0E-06; 7.6E-03 1.4E-02
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 < 0.001 1 2006 2006
dbSNP: rs5275
rs5275
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 < 0.001 1 2015 2015
dbSNP: rs5275
rs5275
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.010 < 0.001 1 2015 2015
dbSNP: rs5275
rs5275
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv
Squamous cell carcinoma of the head and neck
0.010 < 0.001 1 2016 2016
dbSNP: rs689465
rs689465
0.851 0.200 1 186681714 upstream gene variant T/C snv 0.14
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 < 0.001 1 2014 2014
dbSNP: rs689465
rs689465
0.851 0.200 1 186681714 upstream gene variant T/C snv 0.14
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 < 0.001 1 2014 2014
dbSNP: rs689466
rs689466
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.010 < 0.001 1 2015 2015
dbSNP: rs689466
rs689466
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 < 0.001 1 2019 2019
dbSNP: rs689466
rs689466
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 < 0.001 1 2015 2015
dbSNP: rs689466
rs689466
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17
Diabetes Mellitus, Non-Insulin-Dependent
0.010 < 0.001 1 2018 2018
dbSNP: rs689466
rs689466
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 < 0.001 1 2010 2010
dbSNP: rs689466
rs689466
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 < 0.001 1 2010 2010
dbSNP: rs689470
rs689470
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 < 0.001 1 2006 2006
dbSNP: rs689470
rs689470
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 < 0.001 1 2006 2006
dbSNP: rs689470
rs689470
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 < 0.001 1 2006 2006
dbSNP: rs748500299
rs748500299
0.790 0.200 1 186675960 missense variant T/A;C snv 4.0E-06; 4.0E-06
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 < 0.001 1 2015 2015