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: rs7616215
rs7616215
CCR3 ; LOC105377067
0.925 0.280 3 46164194 intron variant C/T snv 0.62
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.810 1.000 1 2013 2015
dbSNP: rs13096142
rs13096142
CCR3
1.000 0.080 3 46240253 intron variant C/T snv 0.25
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2014 2014
dbSNP: rs13098911
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2010 2010
dbSNP: rs7616215
rs7616215
CCR3 ; LOC105377067
0.925 0.280 3 46164194 intron variant C/T snv 0.62
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2011 2011
dbSNP: rs79893749
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10
CUI: C3898105
Disease: Oligoarticular Juvenile Idiopathic Arthritis
Oligoarticular Juvenile Idiopathic Arthritis 		0.800 1.000 1 2013 2013
dbSNP: rs13325613
rs13325613
CCR3
3 46256882 intron variant G/T snv 9.0E-02
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs13325613
rs13325613
CCR3
3 46256882 intron variant G/T snv 9.0E-02
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs3181077
rs3181077
CCR1 ; CCR3
1.000 0.080 3 46209161 intron variant C/T snv 0.80
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs34611049
rs34611049
CCR3
3 46199334 intron variant A/T snv 0.17
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs67676925
rs67676925
CCR3
0.925 0.200 3 46232768 intron variant T/C snv 5.5E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2016 2016
dbSNP: rs67676925
rs67676925
CCR3
0.925 0.200 3 46232768 intron variant T/C snv 5.5E-02
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2016 2016
dbSNP: rs75526024
rs75526024
CCR1 ; CCR3
3 46208969 intron variant A/C snv 4.0E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs79893749
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10
CUI: C2931171
Disease: Juvenile pauciarticular chronic arthritis
Juvenile pauciarticular chronic arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs79893749
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10
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: rs79893749
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10
CUI: C1858558
Disease: Rheumatoid Arthritis, Systemic Juvenile
Rheumatoid Arthritis, Systemic Juvenile 		0.700 1.000 1 2013 2013
dbSNP: rs79893749
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease 		0.700 1.000 1 2013 2013
dbSNP: rs79893749
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10
CUI: C1384600
Disease: Systemic onset juvenile chronic arthritis
Systemic onset juvenile chronic arthritis 		0.700 1.000 1 2013 2013