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: rs6857
rs6857
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.810 1.000 6 2009 2017
dbSNP: rs6859
rs6859
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 10 2008 2019
dbSNP: rs440277
rs440277
1.000 0.080 19 44857967 intron variant G/A snv 0.30
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 4 2009 2019
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: rs1871047
rs1871047
1.000 0.080 19 44848489 intron variant A/G snv 0.31
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 4 2009 2014
dbSNP: rs11673139
rs11673139
1.000 0.080 19 44879780 intron variant A/T snv 8.8E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 3 2009 2012
dbSNP: rs12610605
rs12610605
1.000 0.080 19 44867581 intron variant G/A snv 0.15
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 3 2010 2013
dbSNP: rs3745150
rs3745150
1.000 0.080 19 44882502 intron variant G/C snv 0.35
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 3 2009 2012
dbSNP: rs3852861
rs3852861
1.000 0.080 19 44879804 intron variant G/T snv 0.41
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 3 2011 2014
dbSNP: rs4803763
rs4803763
1.000 0.080 19 44854034 intron variant G/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 3 2009 2012
dbSNP: rs1871046
rs1871046
1.000 0.080 19 44848680 intron variant T/C snv 0.32
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 2 2009 2011
dbSNP: rs283813
rs283813
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 2 2012 2012
dbSNP: rs283813
rs283813
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2012 2012
dbSNP: rs283813
rs283813
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2012 2012
dbSNP: rs377702
rs377702
1.000 0.080 19 44859410 intron variant G/A snv 0.34
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 2 2011 2014
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