Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1064796722 1.000 0.120 17 7676043 missense variant A/C;G snv 1
rs1195793509 1.000 0.120 17 7676210 stop gained -/CATT delins 1
rs1202793339 1.000 0.120 17 7674972 splice acceptor variant C/G;T snv 7.0E-06 1
rs1212996409 1.000 0.120 17 7675197 stop gained T/A;C snv 1
rs1267047192 1.000 0.120 17 7675997 frameshift variant -/C delins 1
rs1555525970 1.000 0.120 17 7675064 stop gained G/A;C snv 1
rs1555526101 1.000 0.120 17 7675115 stop gained G/A;C snv 1
rs1555526466 1.000 0.120 17 7675989 splice region variant C/A;G;T snv 1
rs1555526721 1.000 0.120 17 7676176 stop gained T/A;G snv 1
rs1567541975 1.000 0.120 17 7670664 stop gained C/A snv 1
rs1567542019 1.000 0.120 17 7670673 stop gained C/A snv 1
rs1567542031 1.000 0.120 17 7670673 frameshift variant C/- del 1
rs1567542043 1.000 0.120 17 7670675 frameshift variant TCAGCTCT/- delins 1
rs1567542146 1.000 0.120 17 7670694 frameshift variant -/A ins 1
rs1567542245 1.000 0.120 17 7670706 splice acceptor variant CCCACGGATCTGCAGCAACAGAGGAGGGGGAG/- delins 1
rs1567542299 1.000 0.120 17 7670712 frameshift variant GG/- del 1
rs1567546226 1.000 0.120 17 7673582 frameshift variant AGAGGAGCTG/- delins 1
rs1567546373 1.000 0.120 17 7673595 frameshift variant G/- del 1
rs1567546889 1.000 0.120 17 7673711 frameshift variant -/CCCC delins 1
rs1567547030 1.000 0.120 17 7673728 frameshift variant CGTGG/- del 1
rs1567547066 1.000 0.120 17 7673731 inframe deletion GAGGCTCCCCTTTCTTGCGGAGATTCTCTTCCTCTGTGCGCCGGT/- delins 1
rs1567547687 1.000 0.120 17 7673780 missense variant T/G snv 1
rs1567548114 1.000 0.120 17 7673810 frameshift variant A/- delins 1
rs1567548223 1.000 0.120 17 7673823 frameshift variant C/- delins 1
rs1567548789 1.000 0.120 17 7674159 coding sequence variant -/GGTGGCAAGTGGCTCCTGACCTGGAGTCTTCCAGTGTGATGATGGTGAGGATGGGCCTCCGGTTCATGCCGCCCATG delins 1