rs4845625, IL6R

N. diseases: 9
Source: ALL
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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.800 1.000 2 2013 2018
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.700 1.000 1 2013 2013
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.700 1.000 1 2013 2013
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.030 1.000 3 2011 2014
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.010 1.000 1 2011 2011
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.010 1.000 1 2015 2015
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.010 1.000 1 2015 2015
Hyper LDL cholesterolaemia
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
19 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.010 1.000 1 2015 2015
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.851 0.080 1 154449591 intron variant T/C snv 0.60 0.010 1.000 1 2015 2015