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.
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.800 1.000 1 2014 2014
Autoantibody measurement
CUI: C1272321
Disease: Autoantibody measurement
52 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2009 2009
Body mass index procedure
CUI: C0005893
Disease: Body mass index procedure
252 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2013 2013
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2013 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2011 2011
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
252 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2013 2013
Posterior cortical atrophy syndrome
CUI: C4275079
Disease: Posterior cortical atrophy syndrome
8 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2016 2016
Prion Diseases
CUI: C0162534
Disease: Prion Diseases
67 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2012 2012
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2011 2011
Smoking
CUI: C0037369
Disease: Smoking
765 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2017 2017
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2012 2012
Waist Circumference
CUI: C0455829
Disease: Waist Circumference
183 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2015 2015
Waist-Hip Ratio
CUI: C0205682
Disease: Waist-Hip Ratio
1138 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2015 2015
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