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: rs11865121
rs11865121
1.000 0.080 16 11072831 intron variant C/A snv 0.40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 1 2009 2009
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: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2010 2010
dbSNP: rs12708716
rs12708716
0.807 0.320 16 11086016 intron variant A/G snv 0.37
Diabetes Mellitus, Insulin-Dependent
0.800 1.000 5 2007 2011
dbSNP: rs12924729
rs12924729
0.882 0.200 16 11093926 intron variant G/A snv 0.34
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis
0.700 1.000 1 2011 2011
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: rs887864
rs887864
0.925 0.120 16 11065028 intron variant G/A;C;T snv
CUI: C0018621
Disease: Hay fever
Hay fever
0.700 1.000 1 2011 2011
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
0.800 1.000 1 2012 2012
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
0.810 1.000 1 2011 2013
dbSNP: rs12927355
rs12927355
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2013 2013
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: rs62026376
rs62026376
0.925 0.120 16 11134855 intron variant C/T snv 0.18
CUI: C0004096
Disease: Asthma
Asthma
0.710 1.000 1 2014 2014
dbSNP: rs62026376
rs62026376
0.925 0.120 16 11134855 intron variant C/T snv 0.18
CUI: C0018621
Disease: Hay fever
Hay fever
0.710 1.000 1 2014 2014
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
0.800 1.000 2 2011 2015
dbSNP: rs12927355
rs12927355
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29
Diabetes Mellitus, Insulin-Dependent
0.800 1.000 1 2011 2015
dbSNP: rs2041733
rs2041733
1.000 0.120 16 11135732 intron variant T/C;G snv
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.700 1.000 1 2015 2015
dbSNP: rs3862469
rs3862469
1.000 0.040 16 11100223 intron variant C/T snv 0.35
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
0.700 1.000 1 2015 2015
dbSNP: rs7200786
rs7200786
0.882 0.200 16 11083944 intron variant A/G snv 0.59
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2015 2015
dbSNP: rs12935413
rs12935413
1.000 0.080 16 11116590 intron variant G/A snv 0.34
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs12935413
rs12935413
1.000 0.080 16 11116590 intron variant G/A snv 0.34
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs17229044
rs17229044
1.000 0.120 16 10969079 intron variant C/T snv 0.16
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs34069391
rs34069391
0.925 0.080 16 11067358 intron variant T/- delins
Selective immunoglobulin A deficiency
0.700 1.000 1 2016 2016
dbSNP: rs34069391
rs34069391
0.925 0.080 16 11067358 intron variant T/- delins
Immunoglobulin A deficiency (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs6498168
rs6498168
1.000 0.080 16 11141273 intron variant T/G snv 0.71
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2016 2016
dbSNP: rs8061882
rs8061882
0.827 0.120 16 11067551 intron variant G/C snv 0.11
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016