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: rs13132308
rs13132308
0.807 0.160 4 122629959 intron variant A/G snv 0.10
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 1.000 1 2011 2012
dbSNP: rs6840978
rs6840978
0.776 0.160 4 122633552 intron variant C/T snv 0.16
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.800 1.000 1 2011 2019
dbSNP: rs13132308
rs13132308
0.807 0.160 4 122629959 intron variant A/G snv 0.10
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs13132308
rs13132308
0.807 0.160 4 122629959 intron variant A/G snv 0.10
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs13132308
rs13132308
0.807 0.160 4 122629959 intron variant A/G snv 0.10
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs13132308
rs13132308
0.807 0.160 4 122629959 intron variant A/G snv 0.10
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs13132308
rs13132308
0.807 0.160 4 122629959 intron variant A/G snv 0.10
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs17005934
rs17005934
1.000 0.080 4 122628544 intron variant T/C snv 9.2E-02
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.700 1.000 1 2017 2017
dbSNP: rs62324204
rs62324204
4 122626441 non coding transcript exon variant T/C snv 6.5E-02
CUI: C4505222
Disease: Sleep Onset Latency
Sleep Onset Latency
0.700 1.000 1 2016 2016
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2015 2015
dbSNP: rs62324212
rs62324212
0.724 0.240 4 122639784 intron variant C/A;G snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2015 2015
dbSNP: rs6833591
rs6833591
1.000 0.040 4 122625127 intron variant A/G snv 0.36
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.700 1.000 1 2019 2019