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: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2015 2015
dbSNP: rs11741255
rs11741255
0.724 0.240 5 132475490 intron variant G/A snv 0.29
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2015 2015
dbSNP: rs12515180
rs12515180
5 132449992 intron variant C/T snv 0.28
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs12521868
rs12521868
1.000 0.040 5 132448701 intron variant G/T snv 0.28
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs17622378
rs17622378
0.790 0.200 5 132442760 intron variant A/G snv 0.28
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs17622378
rs17622378
0.790 0.200 5 132442760 intron variant A/G snv 0.28
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1.000 1 2015 2015
dbSNP: rs17622378
rs17622378
0.790 0.200 5 132442760 intron variant A/G snv 0.28
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma
0.700 1.000 1 2019 2019
dbSNP: rs17622378
rs17622378
0.790 0.200 5 132442760 intron variant A/G snv 0.28
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs17622378
rs17622378
0.790 0.200 5 132442760 intron variant A/G snv 0.28
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs17622378
rs17622378
0.790 0.200 5 132442760 intron variant A/G snv 0.28
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs17622517
rs17622517
0.827 0.120 5 132467845 intron variant T/C snv 5.4E-02
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs17622517
rs17622517
0.827 0.120 5 132467845 intron variant T/C snv 5.4E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs17622517
rs17622517
0.827 0.120 5 132467845 intron variant T/C snv 5.4E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs17622517
rs17622517
0.827 0.120 5 132467845 intron variant T/C snv 5.4E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs17622517
rs17622517
0.827 0.120 5 132467845 intron variant T/C snv 5.4E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs2057655
rs2057655
5 132471932 non coding transcript exon variant G/A snv 0.24
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2016 2016
dbSNP: rs2188962
rs2188962
0.882 0.160 5 132435113 intron variant C/T snv 0.29
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs2248116
rs2248116
1.000 0.040 5 132468655 intron variant C/A snv 0.70
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016