Disease: Body mass index
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 4
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 3
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 7
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 4
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 2
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 10
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs5215
KCNJ11
0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 2
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs1899951
PPARG
0.851 0.160 3 12353341 intron variant C/T snv 0.26 2
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 5
rs2237897
KCNQ1
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 2
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 3
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 3