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
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
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
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6