Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs12914385 0.790 0.160 15 78606381 intron variant C/A;T snv 18
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs6570507 0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs667282 0.790 0.120 15 78571130 intron variant T/C snv 0.28 13
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs11030104 0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs3791679 0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs1128249 1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs56113850 0.807 0.080 19 40847202 intron variant T/C snv 0.52 10
rs10968576 0.882 0.120 9 28414341 intron variant A/G snv 0.26 10