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: rs2075650
rs2075650
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: rs157580
rs157580
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: rs2075650
rs2075650
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
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: rs157582
rs157582
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: rs1160985
rs1160985
1.000 0.080 19 44900155 intron variant C/T snv 0.52
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 2 2012 2019
dbSNP: rs1160985
rs1160985
1.000 0.080 19 44900155 intron variant C/T snv 0.52
Low density lipoprotein cholesterol measurement
0.800 1.000 2 2013 2019
dbSNP: rs157580
rs157580
0.882 0.160 19 44892009 intron variant G/A snv 0.69
Low density lipoprotein cholesterol measurement
0.800 1.000 2 2009 2012
dbSNP: rs157582
rs157582
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: rs2075650
rs2075650
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: rs8106922
rs8106922
1.000 0.080 19 44898409 intron variant A/G snv 0.36
Low density lipoprotein cholesterol measurement
0.800 1.000 2 2012 2019
dbSNP: rs8106922
rs8106922
1.000 0.080 19 44898409 intron variant A/G snv 0.36
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs115881343
rs115881343
1.000 0.040 19 44899959 intron variant C/G;T snv 2.9E-02
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
0.710 1.000 1 2014 2014
dbSNP: rs1160984
rs1160984
1.000 0.080 19 44900667 intron variant C/T snv 3.9E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2019 2019
dbSNP: rs1160985
rs1160985
1.000 0.080 19 44900155 intron variant C/T snv 0.52
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2013 2019
dbSNP: rs1160985
rs1160985
1.000 0.080 19 44900155 intron variant C/T snv 0.52
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 1 2013 2019
dbSNP: rs1160985
rs1160985
1.000 0.080 19 44900155 intron variant C/T snv 0.52
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
0.700 1.000 1 2013 2013
dbSNP: rs11668327
rs11668327
1.000 0.080 19 44895376 intron variant G/C snv 0.12
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2018 2018
dbSNP: rs117310449
rs117310449
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: rs157580
rs157580
0.882 0.160 19 44892009 intron variant G/A snv 0.69
High density lipoprotein measurement
0.800 1.000 1 2009 2009
dbSNP: rs157580
rs157580
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: rs157582
rs157582
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
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
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
dbSNP: rs157588
rs157588
19 44895007 intron variant C/T snv 0.59
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018