Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3918226 0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs459193 0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs4919687 0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 9
rs7528419 0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 8
rs604723 1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs633185 0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 8
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs10774625 0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs11066301 0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs112635299 1.000 0.040 14 94371805 downstream gene variant G/T snv 1.3E-02 7
rs13139571 1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs174601 0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 7
rs2681492 0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs11172113 0.882 0.080 12 57133500 intron variant T/C snv 0.42 6
rs12423664 1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6