Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2328529 1.000 0.080 6 20631722 intron variant C/A snv 0.19 1
rs2328531 1.000 0.080 6 20643521 intron variant A/G;T snv 1
rs2328545 1.000 0.080 6 20653319 intron variant G/A;C snv 1
rs2328548 1.000 0.080 6 20716727 intron variant G/A;T snv 1
rs4235999 1.000 0.080 6 20642991 intron variant C/G;T snv 0.39 1
rs4493738 1.000 0.080 6 20775429 intron variant A/G snv 7.5E-02 1
rs4710938 1.000 0.080 6 20640673 intron variant A/G snv 0.42 1
rs4710939 1.000 0.080 6 20644713 intron variant A/G snv 0.41 1
rs4710940 1.000 0.080 6 20657781 intron variant A/C snv 0.46 1
rs4712522 1.000 0.080 6 20656569 intron variant C/G snv 0.40 1
rs4712525 1.000 0.080 6 20662735 intron variant C/G;T snv 1
rs4712526 1.000 0.080 6 20662804 intron variant T/A snv 0.40 1
rs6456364 1.000 0.080 6 20649023 intron variant A/T snv 0.13 1
rs6456367 1.000 0.080 6 20659356 intron variant T/A snv 0.40 1
rs6456369 1.000 0.080 6 20660134 intron variant T/A;C;G snv 1
rs6906327 1.000 0.080 6 20659228 intron variant G/A snv 0.47 1
rs6909558 1.000 0.080 6 20759946 intron variant C/T snv 0.11 1
rs6925328 1.000 0.080 6 20642554 intron variant A/G snv 0.71 1
rs6928012 1.000 0.080 6 20728282 intron variant C/T snv 0.49 1
rs6935599 1.000 0.080 6 20716864 intron variant A/G snv 0.31 1
rs6940200 1.000 0.080 6 20635031 intron variant C/T snv 0.19 1
rs742642 1.000 0.080 6 20664850 intron variant G/A snv 0.21 1
rs7452218 1.000 0.080 6 20767240 intron variant C/T snv 0.11 1
rs7747752 1.000 0.080 6 20725192 intron variant G/C snv 0.34 1
rs7748382 1.000 0.080 6 20665318 intron variant G/A snv 0.41 1