rs2075650, TOMM40

N. diseases: 45
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.
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.020 1.000 2 2013 2017
Alzheimer disease, familial, type 3
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
124 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2017 2017
Behavioral variant of frontotemporal dementia
CUI: C4011788
Disease: Behavioral variant of frontotemporal dementia
10 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2012 2012
Carotid Artery Diseases
CUI: C0007273
Disease: Carotid Artery Diseases
6 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2009 2009
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2014 2014
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2014 2014
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2016 2016
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1 2013 2013
Herpes Simplex Infections
CUI: C0019348
Disease: Herpes Simplex Infections
11 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2018 2018
Hyper LDL cholesterolaemia
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
19 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2015 2015
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2015 2015
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2014 2014
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2014 2014
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2016 2016
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2014 2014
Mild cognitive disorder
CUI: C1270972
Disease: Mild cognitive disorder
96 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2018 2018
Obesity
CUI: C0028754
Disease: Obesity
1111 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2014 2014
Polypoidal choroidal vasculopathy
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
67 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1 2013 2013
Primary Progressive Aphasia (disorder)
CUI: C0282513
Disease: Primary Progressive Aphasia (disorder)
11 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2012 2012
Unipolar Depression
CUI: C0041696
Disease: Unipolar Depression
225 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2014 2014