Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs157588
rs157588
19 44895007 intron variant C/T snv 0.59
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs157588
rs157588
19 44895007 intron variant C/T snv 0.59
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs76366838
rs76366838
19 44896639 intron variant G/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11556510
rs11556510
1.000 0.040 19 44891562 missense variant T/G snv 9.8E-03 1.2E-02
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 < 0.001 1 2011 2011
dbSNP: rs115881343
rs115881343
1.000 0.040 19 44899959 intron variant C/G;T snv 2.9E-02
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.010 1.000 1 2014 2014
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
Mental Disorders 0.710 1.000 1 2014 2014
dbSNP: rs8106922
rs8106922
1.000 0.080 19 44898409 intron variant A/G snv 0.36
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.800 1.000 10 2009 2019
dbSNP: rs405697
rs405697
1.000 0.080 19 44901434 3 prime UTR variant A/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.800 1.000 4 2011 2019
dbSNP: rs10119
rs10119
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 3 2009 2012
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 3 2013 2019
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 3 2012 2019
dbSNP: rs1038026
rs1038026
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2018 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
Nervous System Diseases; Mental Disorders 0.800 1.000 2 2013 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 2 2013 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: rs141864196
rs141864196
1.000 0.080 19 44902242 3 prime UTR variant G/A snv 1.7E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 2 2018 2019
dbSNP: rs760136
rs760136
1.000 0.080 19 44900601 intron variant A/G snv 0.52
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.800 1.000 2 2013 2018
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: rs10119
rs10119
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs10119
rs10119
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs10119
rs10119
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs10119
rs10119
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 < 0.001 1 2011 2011
dbSNP: rs1038025
rs1038025
1.000 0.080 19 44901715 3 prime UTR variant T/C;G snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs1038026
rs1038026
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs1038026
rs1038026
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2013 2013