Source: GWASDB

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: rs12636651
rs12636651
CCR3
3 46240900 intron variant T/C snv 0.32
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs13098911
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs13098911
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs13098911
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		0.700 1.000 1 2011 2011
dbSNP: rs13098911
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2011 2011
dbSNP: rs7652290
rs7652290
CCR3
3 46258274 intron variant A/C;G snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012