Source: BEFREE ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Cervical Squamous Cell Carcinoma
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
44 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2010 2010
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.060 1.000 6 2011 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.050 1.000 5 2011 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
392 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.020 1.000 2 2011 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.020 1.000 2 2012 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
382 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2012 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.030 1.000 3 2013 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
769 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.020 1.000 2 2013 2016
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
53 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2013 2013
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
50 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2013 2013
Conventional (Clear Cell) Renal Cell Carcinoma
203 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2013 2013
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
182 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2013 2013
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
53 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2013 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1022 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.040 1.000 4 2014 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.020 1.000 2 2014 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
2154 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.020 1.000 2 2014 2019
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2014 2014
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
156 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2014 2014
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
456 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2014 2014
Heart failure
CUI: C0018801
Disease: Heart failure
120 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2014 2014
Liver and Intrahepatic Biliary Tract Carcinoma
73 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2014 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
769 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2014 2014
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2014 2014
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
603 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2014 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
616 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2014 2014