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.
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
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
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
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
Longevity
CUI: C0023980
Disease: Longevity
74 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.800 1.000 2 2011 2012
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
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
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
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
Low density lipoprotein cholesterol measurement
1142 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.800 1.000 5 2008 2013
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 4 2008 2013
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.800 1.000 3 2009 2013
High density lipoprotein measurement
1440 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 2 2012 2013
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 2 2012 2013
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 2 2012 2013
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
35 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2013 2013
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
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
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
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
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
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