Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614