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: 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: 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: 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
dbSNP: rs16917237
rs16917237
11 27680836 intron variant G/T snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2015 2015
dbSNP: rs16917237
rs16917237
11 27680836 intron variant G/T snv 0.16
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.700 1.000 1 2018 2018
dbSNP: rs16917237
rs16917237
11 27680836 intron variant G/T snv 0.16
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2019 2019
dbSNP: rs17309874
rs17309874
11 27645689 intron variant G/A snv 0.19
CUI: C0455829
Disease: Waist Circumference
Waist Circumference
0.700 1.000 1 2017 2017
dbSNP: rs2029362
rs2029362
11 27584586 intron variant C/T snv 0.40
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs35051342
rs35051342
11 27612826 intron variant G/C snv 0.16
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2016 2016
dbSNP: rs4517468
rs4517468
11 27666739 intron variant A/T snv 0.53
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs4923460
rs4923460
11 27635242 intron variant G/T snv 0.20
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs4923460
rs4923460
11 27635242 intron variant G/T snv 0.20
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs61888762
rs61888762
11 27688083 intron variant C/G snv 0.27
body fat percentage (physical finding)
0.700 1.000 1 2019 2019
dbSNP: rs6416056
rs6416056
11 27625198 intron variant G/A snv 0.71
CUI: C0005910
Disease: Body Weight
Body Weight
0.700 1.000 1 2017 2017
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: 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: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0562350
Disease: Hip circumference
Hip circumference
0.700 1.000 1 2015 2015