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
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs1014959895 0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1251713297 0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs3480 0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs1057972 0.790 0.200 4 141733279 3 prime UTR variant A/T snv 0.54 7