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: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2009 2009
dbSNP: rs849141
rs849141
0.851 0.240 7 28145472 intron variant A/G snv 0.78
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2009 2009
dbSNP: rs1708299
rs1708299
7 28150327 intron variant A/G snv 0.77
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2010 2010
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: 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: 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: rs1635852
rs1635852
0.882 0.160 7 28149792 intron variant T/C snv 0.42
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2013 2013
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: rs73300638
rs73300638
0.807 0.120 7 28147725 intron variant A/C;G snv
Rheumatoid Arthritis, Systemic Juvenile
0.700 1.000 1 2013 2013
dbSNP: rs73300638
rs73300638
0.807 0.120 7 28147725 intron variant A/C;G snv
Systemic onset juvenile chronic arthritis
0.700 1.000 1 2013 2013
dbSNP: rs73300638
rs73300638
0.807 0.120 7 28147725 intron variant A/C;G snv
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease
0.700 1.000 1 2013 2013
dbSNP: rs73300638
rs73300638
0.807 0.120 7 28147725 intron variant A/C;G snv
Oligoarticular Juvenile Idiopathic Arthritis
0.700 1.000 1 2013 2013
dbSNP: rs73300638
rs73300638
0.807 0.120 7 28147725 intron variant A/C;G snv
Juvenile pauciarticular chronic arthritis
0.700 1.000 1 2013 2013
dbSNP: rs73300638
rs73300638
0.807 0.120 7 28147725 intron variant A/C;G snv
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
0.700 1.000 1 2013 2013
dbSNP: rs917116
rs917116
1.000 0.080 7 28133120 intron variant T/G snv 0.41
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2013 2013
dbSNP: rs552707
rs552707
7 28165684 intron variant T/C snv 0.77
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2014 2014
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: rs849142
rs849142
0.807 0.240 7 28146272 intron variant T/C snv 0.39
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 2 2009 2015
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: 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: rs7808935
rs7808935
1.000 0.080 7 27937744 intron variant T/C snv 0.28
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.700 1.000 1 2015 2015
dbSNP: rs849134
rs849134
1.000 0.080 7 28156603 intron variant A/G snv 0.41
Diabetes Mellitus, Non-Insulin-Dependent
0.800 1.000 2 2010 2016
dbSNP: rs4722762
rs4722762
7 28138643 intron variant G/T snv 0.31
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs860262
rs860262
0.807 0.200 7 28154778 intron variant C/A;T snv 0.41
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016