Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1057519825
BTK
0.882 0.120 X 101356176 missense variant C/G snv 7
rs1057519826
BTK
0.882 0.120 X 101356177 missense variant A/T snv 7
rs2509049 0.827 0.160 11 119095811 upstream gene variant C/A;T snv 6
rs604714 0.925 0.120 11 119099986 intron variant C/A snv 0.31 3
rs121434222
ATM
0.925 0.280 11 108287687 stop gained C/T snv 2
rs121434221 1.000 0.120 11 108329199 missense variant A/G snv 1
rs796051857 1.000 0.120 11 108329181 inframe insertion -/GAA delins 1