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: rs6859219
rs6859219
0.925 0.160 5 56142753 intron variant C/A snv 0.20
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.810 1.000 1 2011 2016
dbSNP: rs6859219
rs6859219
0.925 0.160 5 56142753 intron variant C/A snv 0.20
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.810 1.000 1 2010 2012
dbSNP: rs10065637
rs10065637
1.000 0.040 5 56143024 intron variant C/T snv 0.15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2012 2012
dbSNP: rs10065637
rs10065637
1.000 0.040 5 56143024 intron variant C/T snv 0.15
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1.000 1 2015 2015
dbSNP: rs71624119
rs71624119
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 3 2012 2017
dbSNP: rs71624119
rs71624119
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2016
dbSNP: rs71624119
rs71624119
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2013 2013
dbSNP: rs71624119
rs71624119
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs71624119
rs71624119
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs71624119
rs71624119
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs71624119
rs71624119
0.776 0.200 5 56144903 intron variant G/A snv 0.17
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs10213692
rs10213692
0.807 0.120 5 56146422 intron variant T/C snv 0.17
Rheumatoid Arthritis, Systemic Juvenile
0.700 1.000 1 2013 2013
dbSNP: rs10213692
rs10213692
0.807 0.120 5 56146422 intron variant T/C snv 0.17
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease
0.700 1.000 1 2013 2013
dbSNP: rs10213692
rs10213692
0.807 0.120 5 56146422 intron variant T/C snv 0.17
Juvenile pauciarticular chronic arthritis
0.700 1.000 1 2013 2013
dbSNP: rs10213692
rs10213692
0.807 0.120 5 56146422 intron variant T/C snv 0.17
Systemic onset juvenile chronic arthritis
0.700 1.000 1 2013 2013
dbSNP: rs10213692
rs10213692
0.807 0.120 5 56146422 intron variant T/C snv 0.17
Oligoarticular Juvenile Idiopathic Arthritis
0.700 1.000 1 2013 2013
dbSNP: rs10213692
rs10213692
0.807 0.120 5 56146422 intron variant T/C snv 0.17
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
0.700 1.000 1 2013 2013
dbSNP: rs7731626
rs7731626
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 2 2014 2019
dbSNP: rs7731626
rs7731626
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
0.716 0.240 5 56148856 intron variant G/A snv 0.30
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency
0.700 1.000 1 2015 2015
dbSNP: rs7731626
rs7731626
0.716 0.240 5 56148856 intron variant G/A snv 0.30
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2015 2015