rs2274567, CR1

N. diseases: 10
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.
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 0.700 1.000 1 2012 2012
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 0.010 1.000 1 2014 2014
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 0.010 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 0.010 1.000 1 2009 2009
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 0.010 1.000 1 2019 2019
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 0.010 1.000 1 2019 2019
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 0.010 1.000 1 2019 2019
Malaria
CUI: C0024530
Disease: Malaria
148 0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 0.010 1 2015 2015
Paroxysmal nocturnal hemoglobinuria
CUI: C0024790
Disease: Paroxysmal nocturnal hemoglobinuria
12 0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 0.010 1.000 1 2018 2018
Respiratory Distress Syndrome, Newborn
CUI: C0035220
Disease: Respiratory Distress Syndrome, Newborn
37 0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 0.010 1.000 1 2015 2015