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.
Pemphigus Vulgaris
CUI: C0030809
Disease: Pemphigus Vulgaris
14 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2019 2019
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
Obesity, Morbid
CUI: C0028756
Disease: Obesity, Morbid
48 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.020 1.000 2 2016 2018
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2019 2019
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
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
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
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2017 2017
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2017 2017
Oligospermia
CUI: C0028960
Disease: Oligospermia
71 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2016 2016
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
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
Lymphoma
CUI: C0024299
Disease: Lymphoma
76 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2017 2017
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
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
97 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2019 2019
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
117 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2019 2019
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2019 2019
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
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2019 2019
Male infertility
CUI: C0021364
Disease: Male infertility
137 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.010 1.000 1 2016 2016
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
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
163 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.020 1.000 2 2015 2019
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
167 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.020 1.000 2 2018 2019
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
172 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.020 1.000 2 2018 2019
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