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: rs2903692
rs2903692
0.807 0.360 16 11144926 intron variant G/A snv 0.33
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.840 1.000 4 2007 2010
dbSNP: rs12599402
rs12599402
0.925 0.160 16 11096031 intron variant T/C snv 0.51
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.810 1.000 2 2011 2013
dbSNP: rs12708716
rs12708716
0.807 0.320 16 11086016 intron variant A/G snv 0.37
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.800 1.000 5 2007 2011
dbSNP: rs12924729
rs12924729
0.882 0.200 16 11093926 intron variant G/A snv 0.34
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.800 1.000 3 2011 2015
dbSNP: rs12927355
rs12927355
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.800 1.000 2 2011 2015
dbSNP: rs11865121
rs11865121
1.000 0.080 16 11072831 intron variant C/A snv 0.40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.800 1.000 1 2009 2009
dbSNP: rs12708715
rs12708715
1.000 0.080 16 11083967 intron variant C/T snv 0.39
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs7200786
rs7200786
0.882 0.200 16 11083944 intron variant A/G snv 0.59
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 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
Immune System Diseases 0.800 1.000 1 2013 2013
dbSNP: rs725613
rs725613
0.851 0.240 16 11075826 intron variant T/G snv 0.42
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.740 1.000 4 2007 2013
dbSNP: rs9925481
rs9925481
0.882 0.160 16 11003622 intron variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.730 1.000 4 2009 2011
dbSNP: rs12708716
rs12708716
0.807 0.320 16 11086016 intron variant A/G snv 0.37
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.710 1.000 2 2011 2011
dbSNP: rs17673553
rs17673553
1.000 0.120 16 11148049 intron variant A/G snv 0.18
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.710 1.000 1 2007 2007
dbSNP: rs62026376
rs62026376
0.925 0.120 16 11134855 intron variant C/T snv 0.18
CUI: C0018621
Disease: Hay fever
Hay fever
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.710 1.000 1 2014 2014
dbSNP: rs62026376
rs62026376
0.925 0.120 16 11134855 intron variant C/T snv 0.18
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.710 1.000 1 2014 2014
dbSNP: rs9652601
rs9652601
1.000 0.080 16 11080508 intron variant G/A snv 0.34
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 3 2015 2017
dbSNP: rs11644510
rs11644510
1.000 0.120 16 11183501 downstream gene variant C/T snv 0.39
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 2 2016 2017
dbSNP: rs12935413
rs12935413
1.000 0.080 16 11116590 intron variant G/A snv 0.34
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 2 2011 2012
dbSNP: rs35441874
rs35441874
0.882 0.120 16 11119164 intron variant T/A snv 0.19
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 2 2019 2019
dbSNP: rs7203459
rs7203459
1.000 0.080 16 11136846 intron variant T/C snv 0.23
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 2 2016 2019
dbSNP: rs11644510
rs11644510
1.000 0.120 16 11183501 downstream gene variant C/T snv 0.39
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11645657
rs11645657
1.000 0.080 16 11129597 intron variant C/A;G snv 0.48
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11645657
rs11645657
1.000 0.080 16 11129597 intron variant C/A;G snv 0.48
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11860603
rs11860603
1.000 0.080 16 11071160 intron variant T/C snv 0.41
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2009 2009
dbSNP: rs12599402
rs12599402
0.925 0.160 16 11096031 intron variant T/C snv 0.51
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007