Source: GWASDB

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: rs11669338
rs11669338
1.000 0.080 19 44879727 intron variant T/G snv 8.9E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 1 2009 2018
dbSNP: rs11673139
rs11673139
1.000 0.080 19 44879780 intron variant A/T snv 8.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2012 2018
dbSNP: rs12978931
rs12978931
1.000 0.080 19 44860443 intron variant A/G snv 0.19
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 1 2011 2018
dbSNP: rs519113
rs519113
1.000 0.080 19 44873027 intron variant C/G;T snv
High density lipoprotein measurement
0.800 1.000 1 2011 2011
dbSNP: rs519113
rs519113
1.000 0.080 19 44873027 intron variant C/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 1 2013 2013
dbSNP: rs6857
rs6857
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.800 1.000 1 2013 2013
dbSNP: rs6857
rs6857
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 1 2013 2019
dbSNP: rs6859
rs6859
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2012 2019
dbSNP: rs11667640
rs11667640
1.000 0.080 19 44876534 intron variant C/T snv 7.4E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2011 2011
dbSNP: rs12610605
rs12610605
1.000 0.080 19 44867581 intron variant G/A snv 0.15
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2009 2009
dbSNP: rs12972156
rs12972156
19 44884202 intron variant C/A;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12972970
rs12972970
19 44884339 intron variant G/A snv 0.10
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs1871047
rs1871047
1.000 0.080 19 44848489 intron variant A/G snv 0.31
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2009 2009
dbSNP: rs2075642
rs2075642
19 44874210 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: rs2075642
rs2075642
19 44874210 intron variant G/A;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs2075642
rs2075642
19 44874210 intron variant G/A;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs283813
rs283813
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2009 2009
dbSNP: rs283813
rs283813
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs283813
rs283813
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs34342646
rs34342646
19 44884873 intron variant G/A snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs365653
rs365653
1.000 0.080 19 44858389 intron variant A/G snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs377702
rs377702
1.000 0.080 19 44859410 intron variant G/A snv 0.34
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2009 2009
dbSNP: rs3852856
rs3852856
19 44858317 intron variant G/A;C;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3852856
rs3852856
19 44858317 intron variant G/A;C;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3852856
rs3852856
19 44858317 intron variant G/A;C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012