Disease: Body mass index
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs10795945 1.000 0.080 10 12260608 intergenic variant T/A;C snv 2
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 3
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 7
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 2
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs11671664
GIPR
0.925 0.120 19 45669020 intron variant G/A snv 0.12 2
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 5
rs11709077
PPARG
0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 4
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs1899951
PPARG
0.851 0.160 3 12353341 intron variant C/T snv 0.26 2
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 3
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 2
rs2237897
KCNQ1
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 2
rs2246012
ARG1 ; MED23
1.000 0.080 6 131577068 intron variant T/A;C snv 2
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs2299383
RELN
1.000 0.080 7 103778399 intron variant C/T snv 0.41 2
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5