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: 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
0.700 1.000 2 2018 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: rs10119
rs10119
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2015 2015
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: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2019 2019
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: 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: rs142412517
rs142412517
1.000 0.080 19 44900801 missense variant C/T snv 4.9E-04 5.7E-04
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2019 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: 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
dbSNP: rs157588
rs157588
19 44895007 intron variant C/T snv 0.59
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs2075650
rs2075650
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
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
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
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: rs35568738
rs35568738
1.000 0.080 19 44899461 intron variant G/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2018 2018
dbSNP: rs394819
rs394819
1.000 0.080 19 44901322 missense variant G/A;T snv 3.7E-05; 9.7E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2015 2015
dbSNP: rs561654715
rs561654715
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: rs59007384
rs59007384
0.851 0.080 19 44893408 intron variant G/A;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2014 2014
dbSNP: rs61679753
rs61679753
1.000 0.080 19 44897490 intron variant T/A snv 5.6E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2018 2018
dbSNP: rs71352238
rs71352238
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: rs76692773
rs76692773
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