Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004638 1.000 0.040 9 22115590 intron variant A/C;T snv 3
rs1008878 1.000 0.040 9 22036113 non coding transcript exon variant G/T snv 0.71 2
rs10115049 1.000 0.040 9 22032120 intron variant A/G snv 0.46 2
rs10116277 0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs10120688 0.807 0.080 9 22056500 intron variant G/A snv 0.50 7
rs10127775 1 230160042 intron variant A/G;T snv 4
rs10211524 2 64980940 intron variant G/A snv 0.51 4
rs10217586 1.000 0.040 9 22121350 intron variant A/T snv 0.52 2
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs10500569 16 72722202 intron variant G/A;C;T snv 1
rs10502575 18 31756628 downstream gene variant A/G snv 6.9E-02 1
rs10511701 9 22112600 intron variant T/A;C snv 2
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs10733376 1.000 0.080 9 22114470 intron variant G/C snv 0.64 3
rs10738604 1.000 0.040 9 22025494 intron variant G/A snv 0.29 3
rs10738605 0.925 0.120 9 22049131 non coding transcript exon variant C/A;G snv 3
rs10738606 1.000 0.040 9 22088091 intron variant A/T snv 0.42 2
rs10738607 0.925 0.080 9 22088095 intron variant A/G snv 0.42 4
rs10738609 1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs10757264 1.000 0.040 9 22019733 intron variant A/G snv 0.58 2
rs10757265 1.000 0.040 9 22048860 intron variant T/C snv 0.49 2
rs10757267 1.000 0.040 9 22052811 intron variant G/A;C;T snv 2
rs10757269 1.000 0.040 9 22072265 intron variant A/C;G snv 4
rs10757270 1.000 0.040 9 22072720 intron variant A/C;G snv 0.40 2