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: rs5275
rs5275
0.634 0.321 1 186673926 3 prime UTR variant A/G,T snp 0.40
CUI: C0030193
Disease: Pain
Pain
0.030 1.000 3 2010 2017
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.020 0.500 2 2007 2015
dbSNP: rs5275
rs5275
0.634 0.321 1 186673926 3 prime UTR variant A/G,T snp 0.40
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 1.000 2 2007 2010
dbSNP: rs5275
rs5275
0.634 0.321 1 186673926 3 prime UTR variant A/G,T snp 0.40
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 1.000 2 2007 2010
dbSNP: rs5277
rs5277
0.846 0.107 1 186679065 synonymous variant C/G,T snp 0.12; 8.0E-06 0.12; 3.2E-05
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 1.000 2 2010 2011
dbSNP: rs5277
rs5277
0.846 0.107 1 186679065 synonymous variant C/G,T snp 0.12; 8.0E-06 0.12; 3.2E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 1.000 2 2010 2011
dbSNP: rs5277
rs5277
0.846 0.107 1 186679065 synonymous variant C/G,T snp 0.12; 8.0E-06 0.12; 3.2E-05
CUI: C0030193
Disease: Pain
Pain
0.020 1.000 2 2012 2017
dbSNP: rs689466
rs689466
0.685 0.321 1 186681619 regulatory region variant T/C snp 0.17
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.020 1.000 2 2011 2011
dbSNP: rs689466
rs689466
0.685 0.321 1 186681619 regulatory region variant T/C snp 0.17
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.020 1.000 2 2012 2016
dbSNP: rs689466
rs689466
0.685 0.321 1 186681619 regulatory region variant T/C snp 0.17
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 1.000 2 2012 2016
dbSNP: rs13306035
rs13306035
0.923 0.071 1 186672715 3 prime UTR variant A/G snp
CUI: C1527249
Disease: Colorectal Cancer
Colorectal Cancer
0.010 1.000 1 2010 2010
dbSNP: rs13306035
rs13306035
0.923 0.071 1 186672715 3 prime UTR variant A/G snp
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.010 1.000 1 2011 2011
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0017638
Disease: Glioma
Glioma
0.010 1.000 1 2010 2010
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0235782
Disease: Gallbladder Carcinoma
Gallbladder Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 < 0.001 1 2007 2007
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
Malignant neoplasm of gallbladder
0.010 1.000 1 2011 2011
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2013 2013
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 < 0.001 1 2007 2007
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0014868
Disease: Esophagitis
Esophagitis
0.010 1.000 1 2010 2010
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2013 2013
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2015 2015
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 1.000 1 2010 2010