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: rs193778
rs193778
SOCS1 ; RMI2 ; LOC105371082
1.000 0.120 16 11257354 intron variant A/G snv 0.20
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs367569
rs367569
RMI2 ; LOC105371082
0.807 0.120 16 11271643 intron variant C/T snv 0.32
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs367569
rs367569
RMI2 ; LOC105371082
0.807 0.120 16 11271643 intron variant C/T snv 0.32
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		0.700 1.000 1 2015 2015
dbSNP: rs367569
rs367569
RMI2 ; LOC105371082
0.807 0.120 16 11271643 intron variant C/T snv 0.32
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs367569
rs367569
RMI2 ; LOC105371082
0.807 0.120 16 11271643 intron variant C/T snv 0.32
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs367569
rs367569
RMI2 ; LOC105371082
0.807 0.120 16 11271643 intron variant C/T snv 0.32
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs423674
rs423674
RMI2 ; LOC105371082
0.925 0.120 16 11279548 intron variant G/T snv 0.18
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs423674
rs423674
RMI2 ; LOC105371082
0.925 0.120 16 11279548 intron variant G/T snv 0.18
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs4780355
rs4780355
SOCS1 ; RMI2 ; LOC105371082
0.882 0.120 16 11254001 intron variant T/C;G snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.800 1.000 1 2012 2012
dbSNP: rs4780355
rs4780355
SOCS1 ; RMI2 ; LOC105371082
0.882 0.120 16 11254001 intron variant T/C;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2012 2012
dbSNP: rs12928822
rs12928822
RMI2 ; LOC105371082
0.882 0.200 16 11310036 intron variant C/T snv 0.13
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2010 2010