Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs11651755 0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs7405776 0.807 0.120 17 37733029 intron variant G/A;C snv 6
rs192876988 0.851 0.120 4 79376097 intergenic variant T/C snv 1.6E-02 4