rs429358, APOE

N. diseases: 66
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.
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 2011 2011
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.020 1.000 2 2014 2015
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 2015 2015
Endometrial Hyperplasia
CUI: C0014173
Disease: Endometrial Hyperplasia
6 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 2015 2015
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 1 2016 2016
exudative macular degeneration
CUI: C2237660
Disease: exudative macular degeneration
69 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 1 2016 2016
Geographic Atrophy
CUI: C1536085
Disease: Geographic Atrophy
81 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 1 2016 2016
Hepatolenticular Degeneration
CUI: C0019202
Disease: Hepatolenticular Degeneration
349 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 2018 2018
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 4 2015 2018
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.020 0.500 2 1993 2001
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 1988 1988
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 2018 2018
Hyperlipoproteinemia Type III
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
24 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.730 1.000 3 1988 1994
Hyperlipoproteinemias
CUI: C0020476
Disease: Hyperlipoproteinemias
7 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 1997 1997
Hyperopia
CUI: C0020490
Disease: Hyperopia
29 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 1 2018 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.710 1.000 2 2019 2019
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.040 0.750 4 1993 2004
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 2019 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 2016 2016
Lewy Body Disease
CUI: C0752347
Disease: Lewy Body Disease
41 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 3 2014 2019
Longevity
CUI: C0023980
Disease: Longevity
74 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 1 2019 2019
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 2 2018 2018
Memory performance
CUI: C1285654
Disease: Memory performance
71 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 1 2018 2018
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.710 1.000 2 2017 2019
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.020 0.500 2 2011 2014