Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10468017 0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs4775041 1.000 0.040 15 58382496 intron variant G/C snv 0.24 7
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs8033940 15 58432643 intron variant G/A snv 0.41 5
rs8034802 15 58432593 intron variant T/A snv 0.33 5
rs261336 15 58450219 intron variant G/A snv 0.81 5
rs588136 15 58438299 intron variant C/G;T snv 5
rs473224 15 58445142 intron variant T/A;G snv 5
rs261342 15 58438954 intron variant G/A;C;T snv 5
rs2070895 0.807 0.120 15 58431740 intron variant G/A snv 0.33 5
rs485538 15 58448978 intron variant C/G;T snv 5
rs485671 15 58448935 intron variant A/C;T snv 5
rs261338 15 58442806 intron variant A/G snv 0.83 5
rs2043085 0.827 0.080 15 58388755 intron variant T/C snv 0.54 4
rs6494005 1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38 4
rs572410 15 58449185 intron variant C/G;T snv 4
rs11635491 15 58427542 intron variant G/A snv 0.27 4
rs261341 15 58439368 intron variant A/G snv 0.54 4
rs1077835 15 58431227 intron variant A/G snv 0.34 3
rs261334 15 58434545 intron variant G/C snv 0.73 3
rs13329672 15 58407738 intron variant C/T snv 0.31 1
rs1601935 15 58379566 intron variant G/T snv 0.60 1
rs2043082 15 58382109 intron variant G/A snv 0.32 1