Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 3
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs10994338 0.882 0.040 10 60421370 intron variant G/A snv 7.5E-02 2
rs10994397 0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 2
rs16915157 1.000 0.040 10 60586880 intron variant C/T snv 0.19 1
rs3808943 0.925 0.040 10 60391257 intron variant C/T snv 9.7E-02 1
rs4948418 0.925 0.040 10 60425736 intron variant C/T snv 7.9E-02 1