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: rs9652601
rs9652601
1.000 0.080 16 11080508 intron variant G/A snv 0.34
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
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
0.700 1.000 2 2016 2017
dbSNP: rs35441874
rs35441874
0.882 0.120 16 11119164 intron variant T/A snv 0.19
CUI: C0004096
Disease: Asthma
Asthma
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
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)
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
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
0.700 1.000 1 2018 2018
dbSNP: rs12924112
rs12924112
1.000 0.120 16 11125863 intron variant T/A;G snv
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.700 1.000 1 2019 2019
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: 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: 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: rs12935657
rs12935657
0.925 0.080 16 11125184 intron variant G/A snv 0.18
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs12935657
rs12935657
0.925 0.080 16 11125184 intron variant G/A snv 0.18
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
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: rs17806299
rs17806299
1.000 0.080 16 11106123 intron variant G/A snv 0.15
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2018 2018
dbSNP: rs2041670
rs2041670
0.851 0.280 16 11080795 intron variant G/A;C snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2017 2017
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: rs248831
rs248831
16 11187361 intergenic variant G/A snv 0.31
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
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: rs34972832
rs34972832
0.925 0.120 16 11105081 intron variant G/A;T snv 0.14
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.700 1.000 1 2017 2017
dbSNP: rs34972832
rs34972832
0.925 0.120 16 11105081 intron variant G/A;T snv 0.14
Nodular Sclerosis Classical Hodgkin Lymphoma
0.700 1.000 1 2017 2017
dbSNP: rs35032408
rs35032408
0.925 0.080 16 11121567 intron variant T/C;G snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs35032408
rs35032408
0.925 0.080 16 11121567 intron variant T/C;G snv
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma
0.700 1.000 1 2019 2019