Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs104894396 0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 28
rs1555565774 0.807 0.360 17 44862753 frameshift variant G/- delins 16
rs1561416879 0.925 0.200 5 90629308 stop gained C/G snv 6
rs104893746 0.851 0.120 3 69956460 stop gained C/T snv 6
rs1559751245 0.882 0.280 3 69959280 missense variant C/G snv 6
rs773779627 1.000 0.080 20 59301689 missense variant G/A;T snv 4.0E-06 5
rs768126403 1.000 0.080 13 77918517 stop gained G/A;T snv 4
rs147682682 1.000 0.040 3 69956496 stop gained G/A;T snv 1.2E-05 1.4E-05 4
rs1559749017 0.925 0.040 3 69956531 splice donor variant G/A snv 4