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: 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: 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: 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: rs79589031
rs79589031
7 27894856 intron variant A/G snv 4.4E-02
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs10486567
rs10486567
0.851 0.120 7 27936944 intron variant G/A snv 0.28
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.750 0.857 2 2010 2018
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: 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: rs757138
rs757138
7 27949784 intron variant T/G snv 0.38
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
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: rs6958010
rs6958010
0.925 0.080 7 28099020 intron variant T/G snv 0.79
CUI: C0026654
Disease: Moyamoya Disease
Moyamoya Disease
0.700 1.000 1 2018 2018
dbSNP: rs6958010
rs6958010
0.925 0.080 7 28099020 intron variant T/G snv 0.79
CUI: C2931384
Disease: Moyamoya disease 1
Moyamoya disease 1
0.700 1.000 1 2018 2018
dbSNP: rs78823938
rs78823938
1.000 0.080 7 28101332 intron variant G/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
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: 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: rs57585717
rs57585717
1.000 0.080 7 28109636 intron variant G/A snv 0.25
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs4722758
rs4722758
0.925 0.080 7 28116987 intron variant C/G snv 0.31
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs4722758
rs4722758
0.925 0.080 7 28116987 intron variant C/G snv 0.31
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs6977955
rs6977955
7 28117268 intron variant C/T snv 0.32
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2017 2017
dbSNP: rs9648346
rs9648346
1.000 0.120 7 28120494 intron variant C/A;G snv
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
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: rs917115
rs917115
1.000 0.080 7 28132967 intron variant T/C snv 0.41
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs702814
rs702814
1.000 0.080 7 28133113 intron variant C/T snv 0.37
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2017 2017