Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs117310449
rs117310449
TOMM40
1.000 0.080 19 44890259 intron variant C/T snv 7.3E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
dbSNP: rs561654715
rs561654715
TOMM40
1.000 0.080 19 44890947 intron variant G/A snv 1.7E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
dbSNP: rs76692773
rs76692773
TOMM40
1.000 0.080 19 44890954 intron variant C/T snv 7.5E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
dbSNP: rs71352238
rs71352238
TOMM40
1.000 0.080 19 44891079 intron variant T/C snv 0.10
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
dbSNP: rs157580
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.810 1.000 6 2009 2019
dbSNP: rs157580
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2009 2012
dbSNP: rs157580
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2009 2009
dbSNP: rs157580
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2012 2019
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.900 1.000 11 2009 2020
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 5 2015 2019
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.800 1.000 4 2008 2019
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.830 0.750 2 2012 2015
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.700 1.000 1 2015 2015
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		0.800 1.000 1 2014 2014
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 1 2008 2013
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2015 2015
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2009 2013
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C4275079
Disease: Posterior cortical atrophy syndrome
Posterior cortical atrophy syndrome 		0.700 1.000 1 2016 2016
dbSNP: rs2075650
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0023980
Disease: Longevity
Longevity 		0.800 1.000 1 2011 2012
dbSNP: rs157582
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 3 2016 2019
dbSNP: rs157582
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.810 1.000 2 2010 2019
dbSNP: rs157582
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29
CUI: C0349198
Disease: Acute transient psychotic disorder
Acute transient psychotic disorder 		0.700 1.000 1 2012 2012
dbSNP: rs157582
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2012 2012
dbSNP: rs157582
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29
CUI: C1285654
Disease: Memory performance
Memory performance 		0.700 1.000 1 2017 2017