Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 7
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs17810546 0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs3748816 0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs11712165 0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs10806425 0.851 0.280 6 90216893 intron variant C/A snv 0.33 5