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: rs2041670
rs2041670
0.851 0.280 16 11080795 intron variant G/A;C snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs2058531
rs2058531
1.000 0.080 16 11078252 intron variant T/C snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs2241099
rs2241099
16 11131207 intron variant C/A;G snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs2903692
rs2903692
0.807 0.360 16 11144926 intron variant G/A snv 0.33
Diabetes Mellitus, Insulin-Dependent
0.840 1.000 1 2007 2010
dbSNP: rs6498142
rs6498142
16 10987392 intron variant C/G snv 0.77
CUI: C0202083
Disease: Immunoglobulin A measurement
Immunoglobulin A measurement
0.700 1.000 1 2010 2010
dbSNP: rs7184083
rs7184083
1.000 0.080 16 11134057 intron variant A/G snv 0.72
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2009 2009
dbSNP: rs7200786
rs7200786
0.882 0.200 16 11083944 intron variant A/G snv 0.59
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2007 2007
dbSNP: rs7200786
rs7200786
0.882 0.200 16 11083944 intron variant A/G snv 0.59
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 1 2011 2011
dbSNP: rs7203459
rs7203459
1.000 0.080 16 11136846 intron variant T/C snv 0.23
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.800 1.000 1 2013 2013
dbSNP: rs7203793
rs7203793
1.000 0.080 16 11088277 intron variant C/G;T snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs725613
rs725613
0.851 0.240 16 11075826 intron variant T/G snv 0.42
Diabetes Mellitus, Insulin-Dependent
0.740 1.000 1 2007 2013
dbSNP: rs725613
rs725613
0.851 0.240 16 11075826 intron variant T/G snv 0.42
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2011 2011
dbSNP: rs78394940
rs78394940
16 11128381 intron variant C/G;T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs887864
rs887864
0.925 0.120 16 11065028 intron variant G/A;C;T snv
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.700 1.000 1 2011 2011
dbSNP: rs9302457
rs9302457
1.000 0.080 16 10965980 intron variant G/A snv 0.43
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2011 2011
dbSNP: rs9652582
rs9652582
1.000 0.080 16 11080707 intron variant G/A snv 0.40
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs9746695
rs9746695
1.000 0.080 16 11114037 intron variant T/A;C snv 0.32
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2012 2012
dbSNP: rs9925481
rs9925481
0.882 0.160 16 11003622 intron variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.730 1.000 1 2009 2011
dbSNP: rs9933507
rs9933507
1.000 0.120 16 11107571 intron variant T/C snv 0.46
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2007 2007
dbSNP: rs998592
rs998592
0.925 0.160 16 11105821 intron variant C/T snv 0.39
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2007 2007