Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs17808009
rs17808009
1.000 0.080 12 10159330 3 prime UTR variant C/T snv 0.42
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs3736234
rs3736234
0.851 0.040 12 10160535 non coding transcript exon variant G/A snv 0.40
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3736234
rs3736234
0.851 0.040 12 10160535 non coding transcript exon variant G/A snv 0.40
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3736234
rs3736234
0.851 0.040 12 10160535 non coding transcript exon variant G/A snv 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3736234
rs3736234
0.851 0.040 12 10160535 non coding transcript exon variant G/A snv 0.40
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3736235
rs3736235
0.925 0.080 12 10160476 non coding transcript exon variant T/C snv 0.43 0.40
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs3736235
rs3736235
0.925 0.080 12 10160476 non coding transcript exon variant T/C snv 0.43 0.40
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2010 2010