Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13