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.
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
252 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2015 2015
Memory performance
CUI: C1285654
Disease: Memory performance
71 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2015 2015
Obesity
CUI: C0028754
Disease: Obesity
1111 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.010 1.000 1 2015 2015
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2016 2016
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2016 2016
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
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
988 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2017 2017
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
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
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