Disease: Body mass index
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 3
rs9891146
C17orf58
1.000 0.080 17 67991933 missense variant T/C snv 0.64 0.60 2
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 2
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 3
rs72892910 1.000 0.080 6 50849174 downstream gene variant G/T snv 0.17 2
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 4
rs7144011
NRXN3
1.000 0.080 14 79474040 intron variant G/T snv 0.21 4
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv 3
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 2
rs6947395
AUTS2
1.000 0.080 7 69941675 intron variant A/T snv 0.20 2
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 10
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 4
rs5215
KCNJ11
0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 2
rs4865796
ARL15
1.000 0.080 5 53976834 intron variant G/A snv 0.72 3
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 3
rs35261542
CDKAL1
1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 3