Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518864 0.925 18 55350409 splice acceptor variant C/T snv 7
rs1057518872 0.882 0.160 6 121447287 missense variant T/C snv 5
rs1057518913 0.851 0.320 9 137762822 splice donor variant T/C snv 7
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs1131691299 0.882 0.160 X 41341587 frameshift variant C/- del 9
rs1163944538 0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1164484724 0.790 0.240 9 137108433 stop gained C/T snv 7.0E-06 13
rs121908557 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 23
rs1276519904 0.645 0.520 1 226071445 missense variant A/G snv 63
rs1352010373 0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs1400419650 0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 38
rs149617956 0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 32
rs1553212868 0.807 0.280 1 151406264 frameshift variant G/- delins 17
rs1554032789 0.925 0.160 5 37048547 missense variant T/A snv 13
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs1555154946 0.827 0.120 12 45850644 stop gained C/T snv 16
rs1555386022 0.708 0.320 14 92003418 splice donor variant C/A snv 38
rs1555565774 0.807 0.360 17 44862753 frameshift variant G/- delins 16
rs1558373252 0.790 0.120 2 5693013 frameshift variant T/- delins 19
rs1559470315 0.732 0.320 3 41227287 protein altering variant CCACAAGCAG/T delins 26
rs200661329 0.708 0.440 16 576255 splice donor variant G/A;C snv 5.7E-05 48
rs312262690 0.752 0.320 4 79984831 frameshift variant -/G;GG delins 1.7E-05 28
rs387907260 0.776 0.280 7 66633410 missense variant C/T snv 4.0E-06 1.4E-05 22
rs397516827 0.882 0.160 3 12604194 missense variant G/A;C;T snv 9
rs397517148 0.776 0.200 2 39023128 missense variant C/T snv 27