Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs445925 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 7
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs564398 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 6
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 6
rs10116277 0.827 0.160 9 22081398 intron variant G/T snv 0.62 5
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs523096 0.827 0.080 9 22019130 intron variant A/G snv 0.30 5
rs6475606 0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs7049105 0.807 0.120 9 22028802 intron variant A/G snv 0.58 5
rs7865618 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 5
rs944797 0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 4
rs10120688 0.807 0.080 9 22056500 intron variant G/A snv 0.50 4