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: rs988712
rs988712
0.925 0.160 11 27541835 intron variant G/A;T snv
CUI: C0028754
Disease: Obesity
Obesity
0.810 1.000 1 2011 2018
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0005910
Disease: Body Weight
Body Weight
0.800 1.000 1 2009 2009
dbSNP: rs925946
rs925946
0.882 0.120 11 27645655 intron variant T/G snv 0.72
CUI: C0005910
Disease: Body Weight
Body Weight
0.800 1.000 1 2009 2009
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2009 2019
dbSNP: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2014 2019
dbSNP: rs2049045
rs2049045
1.000 0.080 11 27672694 intron variant G/A;C snv 0.13
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2017 2019
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 2 2010 2019
dbSNP: rs7103411
rs7103411
0.752 0.160 11 27678578 intron variant C/T snv 0.82
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 2 2014 2018
dbSNP: rs10501087
rs10501087
11 27648561 intron variant T/C snv 0.17
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs10767654
rs10767654
11 27618676 intron variant T/G snv 0.73
CUI: C0455829
Disease: Waist Circumference
Waist Circumference
0.700 1.000 1 2017 2017
dbSNP: rs10767654
rs10767654
11 27618676 intron variant T/G snv 0.73
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs10767658
rs10767658
11 27650705 intron variant C/G;T snv
CUI: C0455829
Disease: Waist Circumference
Waist Circumference
0.700 1.000 1 2015 2015
dbSNP: rs10767658
rs10767658
11 27650705 intron variant C/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs10835211
rs10835211
1.000 0.080 11 27679818 intron variant G/A snv 0.19
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs11030100
rs11030100
1.000 0.080 11 27656039 3 prime UTR variant G/T snv 0.17
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs11030102
rs11030102
11 27660049 non coding transcript exon variant C/G snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs11030102
rs11030102
11 27660049 non coding transcript exon variant C/G snv 0.19
CUI: C0005910
Disease: Body Weight
Body Weight
0.700 1.000 1 2017 2017
dbSNP: rs11030104
rs11030104
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs11030108
rs11030108
1.000 0.040 11 27673917 intron variant A/G snv 0.72
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs1519480
rs1519480
0.925 0.040 11 27654165 intron variant C/T snv 0.54
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs1519480
rs1519480
0.925 0.040 11 27654165 intron variant C/T snv 0.54
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs1565228
rs1565228
11 27564889 intron variant G/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs1565228
rs1565228
11 27564889 intron variant G/A;C snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs1565228
rs1565228
11 27564889 intron variant G/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs1565228
rs1565228
11 27564889 intron variant G/A;C snv
High density lipoprotein measurement
0.700 1.000 1 2018 2018