Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691041 17 7676271 frameshift variant -/A delins 3
rs1131691015 17 7676379 splice donor variant -/A delins 1
rs1567542146 1.000 0.120 17 7670694 frameshift variant -/A ins 1
rs1567546818 17 7673707 frameshift variant -/A delins 1
rs1567549651 1.000 0.120 17 7674248 frameshift variant -/A delins 1
rs1567550002 1.000 0.120 17 7674281 frameshift variant -/A delins 1
rs786202514 17 7675096 frameshift variant -/ACCTC delins 1
rs587782609 17 7676211 stop gained -/ATT delins 1
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1267047192 1.000 0.120 17 7675997 frameshift variant -/C delins 1
rs1555523630 1.000 0.120 17 7668202 intron variant -/C delins 1
rs1555525226 17 7673777 frameshift variant -/C ins 1
rs1555526470 1.000 0.120 17 7675992 splice region variant -/C delins 1
rs1567551279 1.000 0.120 17 7674879 frameshift variant -/CACAC delins 1
rs1195793509 1.000 0.120 17 7676210 stop gained -/CATT delins 1
rs1555526784 17 7676244 stop gained -/CCAT delins 1
rs863223301 0.925 0.080 17 7675130 frameshift variant -/CCATGGC delins 2
rs1567546889 1.000 0.120 17 7673711 frameshift variant -/CCCC delins 1
rs1555525158 17 7673757 frameshift variant -/CT delins 1
rs1555525156 17 7673756 frameshift variant -/CTTCTCTTCCTCTGTGC delins 1
rs1555525140 1.000 0.120 17 7673749 frameshift variant -/G delins 1
rs1555527002 1.000 0.120 17 7676556 frameshift variant -/G delins 1
rs1567556454 1.000 0.120 17 7676144 frameshift variant -/G delins 1
rs1131691004 1.000 0.120 17 7676039 frameshift variant -/GAAACCG delins 2
rs1567553717 1.000 0.120 17 7675151 inframe insertion -/GGGCGGGGGTGTGGAATC delins 1