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: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.700 1.000 1 2015 2015
dbSNP: rs755374
rs755374
0.724 0.240 5 159402286 intron variant C/T snv 0.28
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2015 2015