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
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs11651755 0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs8037137 0.807 0.160 15 90963407 upstream gene variant T/C snv 0.19 8
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