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: rs55661102
rs55661102
LPP
0.925 0.080 3 188683350 intron variant A/G snv 0.13
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs55661102
rs55661102
LPP
0.925 0.080 3 188683350 intron variant A/G snv 0.13
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs56116661
rs56116661
LPP
1.000 0.040 3 188683372 intron variant C/T snv 0.25
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2017 2017
dbSNP: rs56116661
rs56116661
LPP
1.000 0.040 3 188683372 intron variant C/T snv 0.25
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1.000 1 2017 2017
dbSNP: rs60946162
rs60946162
LPP
1.000 0.040 3 188415548 intron variant C/T snv 0.35
CUI: C0013595
Disease: Eczema
Eczema
0.700 1.000 1 2019 2019
dbSNP: rs60946162
rs60946162
LPP
1.000 0.040 3 188415548 intron variant C/T snv 0.35
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2017 2017
dbSNP: rs62289742
rs62289742
3 188152990 non coding transcript exon variant C/T snv 0.26
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs6444305
rs6444305
LPP
0.925 0.120 3 188582114 intron variant G/A;C;T snv
CUI: C1334633
Disease: Mature B-Cell Neoplasm
Mature B-Cell Neoplasm
0.700 1.000 1 2014 2014
dbSNP: rs6444307
rs6444307
LPP
3 188589730 intron variant A/G snv 0.33
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs66756607
rs66756607
LPP
1.000 0.080 3 188365131 intron variant T/C snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2013 2013
dbSNP: rs6762714
rs6762714
LPP
1.000 0.080 3 188752450 intron variant C/T snv 0.53
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2016 2016
dbSNP: rs6771736
rs6771736
LPP
1.000 0.040 3 188348649 intron variant C/G snv 0.68
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2018 2018
dbSNP: rs73194495
rs73194495
LPP
1.000 0.080 3 188610688 intron variant A/T snv 0.15
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs73196739
rs73196739
LPP
0.925 0.120 3 188684683 intron variant C/T snv 0.13
CUI: C0013595
Disease: Eczema
Eczema
0.700 1.000 1 2019 2019
dbSNP: rs73196739
rs73196739
LPP
0.925 0.120 3 188684683 intron variant C/T snv 0.13
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2016 2016
dbSNP: rs80236973
rs80236973
LPP
3 188283226 intron variant C/T snv 9.6E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs9815073
rs9815073
LPP
0.925 0.120 3 188397894 intron variant C/A;G snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.700 1.000 1 2016 2016
dbSNP: rs9815073
rs9815073
LPP
0.925 0.120 3 188397894 intron variant C/A;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs9815073
rs9815073
LPP
0.925 0.120 3 188397894 intron variant C/A;G snv
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma
0.700 1.000 1 2016 2016
dbSNP: rs9815874
rs9815874
LPP
3 188723373 intron variant C/T snv 0.21
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs9830664
rs9830664
LPP
1.000 0.080 3 188874357 missense variant G/A snv 2.1E-03 2.5E-03
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018
dbSNP: rs9852988
rs9852988
LPP
1.000 0.080 3 188327228 intron variant A/G snv 0.11
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs9860547
rs9860547
LPP
0.925 0.080 3 188411191 intron variant G/A snv 0.34
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs9860547
rs9860547
LPP
0.925 0.080 3 188411191 intron variant G/A snv 0.34
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs9864529
rs9864529
LPP
1.000 0.040 3 188387268 intron variant G/A snv 0.52
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
0.700 1.000 1 2015 2015