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: rs2903692
rs2903692
0.784 0.321 16 11144926 intron variant G/A snp 0.33
Diabetes Mellitus, Insulin-Dependent
0.840 1.000 1 2007 2010
dbSNP: rs12708716
rs12708716
0.784 0.250 16 11086016 intron variant A/G snp 0.37
Diabetes Mellitus, Insulin-Dependent
0.800 5 2007 2011
dbSNP: rs11865121
rs11865121
1.000 0.071 16 11072831 intron variant C/A snp 0.40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1 2009 2009
dbSNP: rs12599402
rs12599402
0.923 0.143 16 11096031 intron variant T/C snp 0.50
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.800 1 2013 2013
dbSNP: rs12924729
rs12924729
0.878 0.143 16 11093926 intron variant G/A snp 0.34
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis
0.800 1 2011 2012
dbSNP: rs12927355
rs12927355
0.878 0.179 16 11100914 intron variant C/T snp 0.29
Diabetes Mellitus, Insulin-Dependent
0.800 1 2012 2015
dbSNP: rs6498142
rs6498142
16 10987392 intron variant C/G snp 0.78
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.800 1 2010 2010
dbSNP: rs7200786
rs7200786
0.878 0.179 16 11083944 intron variant A/G snp 0.58
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1 2011 2011
dbSNP: rs7203459
rs7203459
1.000 0.071 16 11136846 intron variant T/C snp 0.22
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
0.800 1 2013 2013
dbSNP: rs12927355
rs12927355
0.878 0.179 16 11100914 intron variant C/T snp 0.29
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.710 1.000 1 2014 2016
dbSNP: rs62026376
rs62026376
0.923 0.107 16 11134855 intron variant C/T snp 0.18
CUI: C0004096
Disease: Asthma
Asthma
0.710 1.000 1 2014 2014
dbSNP: rs62026376
rs62026376
0.923 0.107 16 11134855 intron variant C/T snp 0.18
CUI: C0018621
Disease: Hay fever
Hay fever
0.710 1.000 1 2014 2014
dbSNP: rs11644510
rs11644510
16 11183501 C/T snp 0.39
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity
0.700 2 2017 2017
dbSNP: rs9652601
rs9652601
1.000 0.071 16 11080508 intron variant G/A snp 0.34
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 2 2016 2017
dbSNP: rs12708715
rs12708715
0.923 0.036 16 11083967 intron variant C/T snp 0.38
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1 2012 2012
dbSNP: rs12924729
rs12924729
0.878 0.143 16 11093926 intron variant G/A snp 0.34
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1 2016 2016
dbSNP: rs12935413
rs12935413
1.000 0.036 16 11116590 intron variant G/A snp 0.34
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1 2017 2017
dbSNP: rs12935413
rs12935413
1.000 0.036 16 11116590 intron variant G/A snp 0.34
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1 2017 2017
dbSNP: rs12935413
rs12935413
1.000 0.036 16 11116590 intron variant G/A snp 0.34
CUI: C0750879
Disease: Eosinophil count result
Eosinophil count result
0.700 1 2017 2017
dbSNP: rs17229044
rs17229044
1.000 0.107 16 10969079 intron variant C/T snp 0.16
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1 2017 2017
dbSNP: rs17806299
rs17806299
1.000 0.071 16 11106123 intron variant G/A snp 0.15
CUI: C0004096
Disease: Asthma
Asthma
0.700 1 2018 2018
dbSNP: rs2041733
rs2041733
1.000 0.107 16 11135732 intron variant T/C,G snp 0.54
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.700 1 2016 2016
dbSNP: rs34069391
rs34069391
1.000 0.071 16 11067358 intron variant GT/G in-del
Immunoglobulin A deficiency (disorder)
0.700 1 2016 2016
dbSNP: rs34972832
rs34972832
0.923 0.107 16 11105081 intron variant G/A snp 0.14
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.700 1 2017 2017
dbSNP: rs34972832
rs34972832
0.923 0.107 16 11105081 intron variant G/A snp 0.14
Nodular Sclerosis Classical Hodgkin Lymphoma
0.700 1 2017 2017