Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81