Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 7
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 2
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 1
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 1
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 1
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 1
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2