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: 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: rs529866
rs529866
RMI2 ; LOC105371082
1.000 0.040 16 11279463 intron variant C/T snv 0.18
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 2 2012 2017
dbSNP: rs1646019
rs1646019
RMI2 ; LOC105371082
1.000 0.080 16 11265823 intron variant C/T snv 0.36
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.800 1.000 1 2012 2012
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: rs529866
rs529866
RMI2 ; LOC105371082
1.000 0.040 16 11279463 intron variant C/T snv 0.18
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2017 2017
dbSNP: rs6498184
rs6498184
RMI2 ; LOC105371082 ; LOC105371083
1.000 0.080 16 11342133 non coding transcript exon variant T/A;C snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
dbSNP: rs7191700
rs7191700
RMI2 ; LOC105371082
1.000 0.080 16 11312946 intron variant C/T snv 0.27
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs77061563
rs77061563
RMI2 ; LOC105371082
1.000 0.040 16 11358685 intron variant C/G;T snv
CUI: C0023343
Disease: Leprosy
Leprosy 		0.700 1.000 1 2015 2015
dbSNP: rs77804393
rs77804393
RMI2 ; LOC105371082
1.000 0.040 16 11265296 intron variant G/A;T snv
CUI: C0013595
Disease: Eczema
Eczema 		0.700 1.000 1 2019 2019
dbSNP: rs80073729
rs80073729
RMI2 ; LOC105371082
1.000 0.080 16 11279940 intron variant G/A snv 4.1E-03
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012