rs4420638, APOC1

N. diseases: 43
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.
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.800 1.000 16 2007 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.820 1.000 11 2007 2019
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.800 1.000 7 2009 2019
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.800 1.000 7 2010 2019
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.810 1.000 2 2013 2019
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.710 1.000 2 2012 2019
Waist-Hip Ratio
CUI: C0205682
Disease: Waist-Hip Ratio
1138 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 2 2018 2019
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.010 1.000 1 2019 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.800 1.000 8 2009 2018
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.800 1.000 5 2007 2018
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.010 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2017 2017
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
988 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2017 2017
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
988 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2017 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.820 1.000 4 2009 2016
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 2 2015 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.710 1.000 2 2013 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.710 1.000 2 2013 2016
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2016 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2016 2016
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2016 2016
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2016 2016
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2016 2016
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2016 2016
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2016 2016