Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1114167302 0.925 0.320 17 58216687 missense variant C/A snv 2
rs1331874836 0.925 0.320 14 88857230 missense variant G/T snv 7.0E-06 2
rs1376664664 0.882 0.320 17 58214739 splice donor variant A/C;G snv 4.1E-06 3
rs1487082103 0.925 0.320 19 41354927 missense variant T/G snv 8.2E-06 2
rs1488635637 0.827 0.360 17 58208003 splice acceptor variant T/C;G snv 7.0E-06 6
rs1555596845 0.882 0.320 17 58206493 frameshift variant GTGACAGTGCCTGTGGTCTCTGTGCGGAG/- delins 3
rs1555596943 0.882 0.320 17 58206549 splice acceptor variant T/C snv 3
rs1555599412 0.827 0.320 17 58213011 stop gained C/A snv 5
rs1555601787 0.882 0.320 17 58219230 start lost T/C snv 3
rs199874059 0.882 0.320 17 58210658 splice donor variant C/T snv 6.0E-05 2.1E-05 3
rs201845154 1.000 0.320 17 58214760 missense variant G/A snv 1.8E-04 3.4E-04 1
rs201933838 0.882 0.320 17 58214740 splice donor variant C/T snv 1.2E-05 3
rs281797258 0.882 0.400 20 10413265 missense variant G/A snv 4.0E-06 2.4E-04 3
rs375170572 0.827 0.320 17 58218618 splice donor variant A/G snv 3.2E-05 3.5E-05 5
rs375431319 0.925 0.320 3 97780679 missense variant T/C snv 2
rs386834043 0.851 0.320 17 58206553 splice region variant ATGCCATTGGGACAGCCTCAGGTTTCTGC/- delins 1.3E-03 4
rs386834044 0.851 0.320 17 58206501 frameshift variant -/CCTG delins 7.2E-05 7.0E-06 4
rs386834046 0.882 0.320 17 58218620 frameshift variant AGTTGGC/- delins 3
rs386834048 0.827 0.320 17 58216088 splice region variant C/T snv 1.3E-04 1.3E-04 5
rs386834051 0.882 0.320 17 58219175 frameshift variant -/CCCGG delins 6.6E-06 3
rs386834052 0.882 0.320 17 58219149 splice donor variant A/G snv 3
rs386834053 0.925 0.320 17 58210980 missense variant C/T snv 2.0E-05 2.1E-05 2
rs730880323 1.000 0.320 17 58219176 frameshift variant -/CCGGG delins 1
rs74315394 0.851 0.440 20 10412791 missense variant C/A snv 5.2E-03 5.0E-03 4
rs754279998 0.776 0.360 17 58208153 inframe deletion GAG/- delins 2.0E-05 1.4E-05 10