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: rs10781499
rs10781499
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.800 1.000 3 2011 2017
dbSNP: rs10781499
rs10781499
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 2 2012 2017
dbSNP: rs10781500
rs10781500
1.000 0.040 9 136374886 upstream gene variant C/G;T snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.800 1.000 1 2011 2011
dbSNP: rs4077515
rs4077515
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2010 2010
dbSNP: rs4077515
rs4077515
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.800 1.000 1 2010 2010
dbSNP: rs10870077
rs10870077
0.827 0.120 9 136369439 intron variant C/G snv 0.38
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.710 1.000 1 2008 2016
dbSNP: rs10870077
rs10870077
0.827 0.120 9 136369439 intron variant C/G snv 0.38
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.710 1.000 1 2008 2016
dbSNP: rs4077515
rs4077515
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.710 1.000 1 2014 2017
dbSNP: rs10781499
rs10781499
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 2 2015 2017
dbSNP: rs10870077
rs10870077
0.827 0.120 9 136369439 intron variant C/G snv 0.38
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs10870077
rs10870077
0.827 0.120 9 136369439 intron variant C/G snv 0.38
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs10870077
rs10870077
0.827 0.120 9 136369439 intron variant C/G snv 0.38
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs10870202
rs10870202
9 136362959 intron variant T/C snv 0.48 0.48
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2017 2017
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2015 2015
dbSNP: rs11145763
rs11145763
0.724 0.240 9 136369144 intron variant A/C;G;T snv
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
0.700 1.000 1 2015 2015