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 16
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 15
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 4