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: rs3749171
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 1 2012 2012
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.800 1.000 1 2013 2013
dbSNP: rs3749171
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.710 1.000 3 2015 2019
dbSNP: rs3749172
rs3749172
GPR35
1.000 0.040 2 240630832 missense variant A/C;T snv 0.56; 2.0E-05
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.710 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.710 1.000 1 2009 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 2 2013 2015
dbSNP: rs34236350
rs34236350
GPR35
2 240628909 5 prime UTR variant C/T snv 0.25
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs34236350
rs34236350
GPR35
2 240628909 5 prime UTR variant C/T snv 0.25
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs3749171
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs3749171
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs3749171
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs3749171
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs4676410
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2015 2015