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: rs1635852
rs1635852
0.882 0.160 7 28149792 intron variant T/C snv 0.42
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.800 1.000 1 2013 2013
dbSNP: rs67250450
rs67250450
1.000 0.120 7 28135367 intron variant T/C snv 0.31
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 1 2014 2014
dbSNP: rs864745
rs864745
0.763 0.320 7 28140937 intron variant T/C snv 0.41
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2012 2012
dbSNP: rs1635852
rs1635852
0.882 0.160 7 28149792 intron variant T/C snv 0.42
Diabetes Mellitus, Non-Insulin-Dependent
0.710 1.000 1 2013 2019
dbSNP: rs10225163
rs10225163
0.925 0.120 7 27886026 intron variant C/G snv 0.53
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 1 2012 2012
dbSNP: rs10225163
rs10225163
0.925 0.120 7 27886026 intron variant C/G snv 0.53
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 1 2012 2012
dbSNP: rs10245867
rs10245867
0.925 0.080 7 28102567 intron variant G/T snv 0.37
CUI: C0013595
Disease: Eczema
Eczema
0.700 1.000 1 2019 2019
dbSNP: rs10245867
rs10245867
0.925 0.080 7 28102567 intron variant G/T snv 0.37
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2017 2017
dbSNP: rs10274928
rs10274928
7 28102469 intron variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs10276381
rs10276381
1.000 0.040 7 28150502 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2015 2015
dbSNP: rs1029534
rs1029534
7 28149464 intron variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2013 2013
dbSNP: rs10486567
rs10486567
0.851 0.120 7 27936944 intron variant G/A snv 0.28
Prostate specific antigen measurement
0.700 1.000 1 2017 2017
dbSNP: rs11495981
rs11495981
1.000 0.120 7 28137682 intron variant C/T snv 0.29
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.700 1.000 1 2019 2019
dbSNP: rs11495981
rs11495981
1.000 0.120 7 28137682 intron variant C/T snv 0.29
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases
0.700 1.000 1 2019 2019
dbSNP: rs11973028
rs11973028
1.000 0.120 7 27853217 intron variant C/T snv 0.44
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.700 1.000 1 2019 2019
dbSNP: rs11981911
rs11981911
0.925 0.040 7 27848395 intron variant C/T snv 0.44
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs11981911
rs11981911
0.925 0.040 7 27848395 intron variant C/T snv 0.44
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 1.000 1 2018 2018
dbSNP: rs12531540
rs12531540
1.000 0.080 7 28123055 intron variant C/T snv 0.36
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2015 2015
dbSNP: rs13247499
rs13247499
7 28139639 intron variant C/A snv 0.10
Alanine aminotransferase measurement
0.700 1.000 1 2018 2018
dbSNP: rs13247499
rs13247499
7 28139639 intron variant C/A snv 0.10
Serum Alanine Aminotransferase Measurement
0.700 1.000 1 2018 2018
dbSNP: rs1513272
rs1513272
7 28160478 intron variant C/T snv 0.40
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs1513272
rs1513272
7 28160478 intron variant C/T snv 0.40
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs1513272
rs1513272
7 28160478 intron variant C/T snv 0.40
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2019 2019
dbSNP: rs1557779
rs1557779
7 27955139 intron variant T/C snv 0.85
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1635851
rs1635851
7 28148187 intron variant C/T snv 0.55
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017