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: rs11549428
rs11549428
SOCS1 ; RMI2 ; LOC105371082
16 11254849 missense variant C/G;T snv 5.0E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs11643024
rs11643024
RMI2 ; LOC105371082
16 11349326 intron variant A/G snv 0.67
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs11643024
rs11643024
RMI2 ; LOC105371082
16 11349326 intron variant A/G snv 0.67
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs35578928
rs35578928
RMI2 ; LOC400499 ; LOC105371082
16 11373920 intron variant G/A snv 0.15
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs4781072
rs4781072
RMI2 ; LOC105371082
16 11366623 intron variant C/G;T snv
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs7188861
rs7188861
RMI2 ; LOC105371082
16 11360793 intron variant C/A snv 0.16
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2015 2015
dbSNP: rs8061370
rs8061370
RMI2 ; LOC105371082
0.882 16 11364614 intron variant A/C;T snv
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs8061370
rs8061370
RMI2 ; LOC105371082
0.882 16 11364614 intron variant A/C;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs8061370
rs8061370
RMI2 ; LOC105371082
0.882 16 11364614 intron variant A/C;T snv
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs8061370
rs8061370
RMI2 ; LOC105371082
0.882 16 11364614 intron variant A/C;T snv
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
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: 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: 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: 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: 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: 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
dbSNP: rs367569
rs367569
RMI2 ; LOC105371082
0.807 0.120 16 11271643 intron variant C/T snv 0.32
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.800 1.000 2 2012 2016
dbSNP: rs11074967
rs11074967
RMI2 ; LOC400499 ; LOC105371082
0.807 0.120 16 11377557 intron variant C/G snv 0.36
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease 		0.700 1.000 1 2013 2013
dbSNP: rs11074967
rs11074967
RMI2 ; LOC400499 ; LOC105371082
0.807 0.120 16 11377557 intron variant C/G snv 0.36
CUI: C1858558
Disease: Rheumatoid Arthritis, Systemic Juvenile
Rheumatoid Arthritis, Systemic Juvenile 		0.700 1.000 1 2013 2013
dbSNP: rs11074967
rs11074967
RMI2 ; LOC400499 ; LOC105371082
0.807 0.120 16 11377557 intron variant C/G snv 0.36
CUI: C2931171
Disease: Juvenile pauciarticular chronic arthritis
Juvenile pauciarticular chronic arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs11074967
rs11074967
RMI2 ; LOC400499 ; LOC105371082
0.807 0.120 16 11377557 intron variant C/G snv 0.36
CUI: C1384600
Disease: Systemic onset juvenile chronic arthritis
Systemic onset juvenile chronic arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs11074967
rs11074967
RMI2 ; LOC400499 ; LOC105371082
0.807 0.120 16 11377557 intron variant C/G snv 0.36
CUI: C3890205
Disease: Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative 		0.700 1.000 1 2013 2013
dbSNP: rs11074967
rs11074967
RMI2 ; LOC400499 ; LOC105371082
0.807 0.120 16 11377557 intron variant C/G snv 0.36
CUI: C3898105
Disease: Oligoarticular Juvenile Idiopathic Arthritis
Oligoarticular Juvenile Idiopathic Arthritis 		0.700 1.000 1 2013 2013