Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs715 1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 12
rs7740107 1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs34720381 1 171486183 intron variant C/T snv 7.3E-02 4
rs6809651 3 186096853 intron variant G/A snv 0.14 4
rs10513801 3 186104564 intron variant T/G snv 9.2E-02 3
rs6968554 7 17247482 5 prime UTR variant A/G;T snv 2
rs6973656 7 77793266 downstream gene variant A/G;T snv 2
rs72817412 16 89075082 intergenic variant C/A;T snv 2