Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201408539 0.827 0.080 17 46088713 intron variant TA/- delins 6
rs7225002 0.925 0.080 17 46111701 intron variant A/G snv 0.39 5
rs148910659 17 46055293 intron variant G/A snv 3
rs78746179 17 46127240 intron variant C/T snv 5.0E-02 2
rs35524223 17 46115224 intron variant T/A snv 0.14 2
rs776509440 17 46096136 intron variant -/CTT;CTTT;CTTTT;CTTTTT;CTTTTTT;CTTTTTTT;CTTTTTTTT;CTTTTTTTTTT;CTTTTTTTTTTTTTTT delins 2
rs11654745 17 46053730 intron variant G/A snv 0.35 2
rs2696579 17 46150027 intron variant T/A;C snv 2
rs142920272 17 46224474 intron variant T/A;C snv 1
rs8080583 17 46085231 intron variant C/A snv 0.23 1
rs17577094 0.925 0.120 17 46110126 intron variant A/G snv 0.14 1
rs4606752 17 46115252 intron variant A/G snv 0.14 1
rs2532263 1.000 0.080 17 46175102 intron variant G/A snv 0.12 1
rs115231027 17 46121924 intron variant T/C snv 1
rs11653367 17 46114117 intron variant A/G;T snv 1