Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.679 0.107 12 2236129 intron variant G/A snp 0.37 13
rs8321 0.734 0.250 6 30064745 3 prime UTR variant A/C snp 5.4E-02 6.5E-02 13
rs3129817 0.724 0.286 6 30374976 intergenic variant G/A snp 0.12 12
rs1480380 0.744 0.321 6 32945469 intron variant C/T snp 0.11 10
rs11191580 0.821 0.036 10 103146454 intron variant T/C snp 8.2E-02 8
rs9275524 0.784 0.143 6 32707332 intergenic variant T/C snp 0.57 7
rs8042374 0.784 0.107 15 78615690 intron variant A/G snp 0.29 7
rs3129939 0.801 0.286 6 32368989 intron variant A/G snp 0.15 7
rs2252865 0.821 0.036 1 8362616 intron variant T/C snp 0.71 6
rs412657 0.821 0.250 6 32243308 intergenic variant T/C,G snp 0.52 5
rs7004633 0.821 0.036 8 88748082 intergenic variant A/G snp 0.26 5
rs9951150 0.821 0.036 18 55153893 intergenic variant A/G,T snp 0.50 5
rs10994359 0.801 0.036 10 60462349 intron variant T/C snp 9.2E-02 5
rs10994397 0.821 0.036 10 60519366 intron variant C/T snp 0.11 5
rs6265 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 5
rs2799573 0.821 0.036 10 18312999 intron variant T/C snp 0.21 5
rs7914558 0.821 0.036 10 103016151 intron variant G/A snp 0.41 5
rs10503253 0.821 0.036 8 4323322 intron variant C/A snp 0.20 5
rs2535629 0.801 0.036 3 52799203 intron variant G/A,C snp 0.45 5
rs12966547 0.801 0.036 18 55084786 regulatory region variant G/A snp 0.40 5
rs9297357 0.821 0.036 8 105130105 intron variant C/G,T snp 0.74 5
rs11191454 0.821 0.036 10 102900247 intron variant A/G snp 8.2E-02 5
rs17662626 0.821 0.036 2 193119895 intergenic variant A/G snp 5.7E-02 5
rs1625579 0.784 0.036 1 98037378 intron variant G/T snp 0.77 5
rs2721800 0.821 0.036 7 24652933 intron variant G/A,C,T snp 0.16; 1.2E-03 5