Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908212 0.732 0.160 19 13303877 missense variant G/A snv 14
rs121908225 0.790 0.120 19 13365448 missense variant G/A snv 12
rs1057520918 0.790 0.160 19 13262780 missense variant C/T snv 11
rs121909323 0.790 0.160 19 13277122 stop gained G/A snv 8
rs121908216 0.882 0.200 19 13235702 missense variant C/T snv 7
rs786200962 0.827 0.120 19 13298768 frameshift variant A/- del 7
rs786200963 0.827 0.200 19 13371683 splice region variant C/T snv 6
rs886037945 0.827 0.160 19 13303584 missense variant C/T snv 6
rs121908247 0.851 0.160 19 13235693 missense variant C/T snv 5
rs794727411 0.851 0.160 19 13261526 missense variant C/G;T snv 5
rs121909324 0.851 0.160 19 13255217 stop gained G/A snv 4
rs121908215 0.882 0.160 19 13359707 missense variant C/T snv 3
rs121909326 0.882 0.160 19 13235219 missense variant A/G snv 3
rs1568440440 0.925 0.120 19 13228767 stop gained GT/- delins 3
rs863224852 0.882 0.160 19 13359680 missense variant C/T snv 3
rs121908226 0.925 0.120 19 13231847 missense variant C/T snv 2
rs121908236 0.925 0.160 19 13359724 missense variant C/T snv 2
rs1272886269 0.925 0.120 19 13335805 splice donor variant C/T snv 4.2E-06 2
rs1555737113 0.925 0.120 19 13231850 missense variant C/T snv 2
rs1555743942 0.925 0.120 19 13257514 stop gained G/A snv 2
rs1555755909 0.925 0.120 19 13298704 frameshift variant GCTCCGCCTTGTCCTCCGGACCCTCC/- delins 2
rs1555756130 0.925 0.120 19 13298878 stop gained C/A snv 2
rs1555756461 0.925 0.120 19 13299314 frameshift variant CAC/GT delins 2
rs1555756737 0.925 0.120 19 13300638 stop gained C/A snv 2
rs1555757523 0.925 0.120 19 13303832 frameshift variant T/- del 2