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's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.900 1.000 33 2009 2020
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.830 0.750 4 2012 2015
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.800 1.000 5 2008 2019
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: 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 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
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
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
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.710 1.000 2 2013 2017
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 5 2015 2019
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
High density lipoprotein measurement
CUI: C0392885
Disease: 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
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