Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1537372 0.752 0.120 9 22103184 intron variant G/A;T snv 14
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs7865618 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 11
rs445925 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs751093906 0.882 0.200 8 42472255 stop gained G/A;C snv 4.0E-06 8
rs1537375 0.882 0.120 9 22116072 intron variant T/C;G snv 6
rs2383204 0.827 0.160 9 22055049 intron variant A/G;T snv 6
rs9632884 0.851 0.160 9 22072302 intron variant G/A;C snv 6
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs3218020 0.882 0.120 9 21997873 intron variant G/A;C snv 5
rs10127775 1 230160042 intron variant A/G;T snv 4
rs10757269 1.000 0.040 9 22072265 intron variant A/C;G snv 4
rs1440581 1.000 0.080 4 88305270 intron variant T/A;C snv 4
rs1912826 4 186228386 intron variant G/A;C snv 4
rs7857345 0.925 0.080 9 22087474 non coding transcript exon variant T/A;C snv 4
rs944801 0.882 0.120 9 22051671 intron variant G/A;C snv 4
rs1004638 1.000 0.040 9 22115590 intron variant A/C;T snv 3
rs10738605 0.925 0.120 9 22049131 non coding transcript exon variant C/A;G snv 3
rs10738609 1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs10811647 1.000 0.040 9 22065003 intron variant C/G;T snv 3
rs10965212 0.925 0.080 9 22023796 intron variant T/A;C;G snv 3