Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386833981 0.925 0.120 13 77000517 missense variant T/G snv 3
rs104894386 0.925 0.120 13 76995077 missense variant G/A;C snv 8.0E-06 2
rs386833975 0.925 0.120 13 76995990 missense variant A/G snv 2
rs546989392 0.925 0.120 13 76996010 stop gained C/T snv 2.0E-05 7.7E-05 2
rs104894385 0.925 0.120 13 76992176 stop gained G/A;T snv 2.7E-05; 3.1E-05 2
rs1555274338 1.000 0.120 13 77000567 stop gained G/A;C snv 2
rs28940280 0.925 0.120 13 77000580 missense variant G/A snv 8.0E-06 2
rs386833966 0.925 0.120 13 77000824 frameshift variant T/- delins 2
rs386833967 0.925 0.120 13 77000845 frameshift variant AACA/- delins 2.8E-05 2
rs386833969 0.925 0.120 13 77000918 frameshift variant AT/- delins 2
rs386833979 0.925 0.120 13 76996083 frameshift variant -/C delins 2
rs386833980 0.925 0.120 13 76996086 stop gained G/A snv 1.6E-05 3.5E-05 2
rs587780315 1.000 0.120 13 76996086 frameshift variant G/- delins 2
rs786204644 0.925 0.120 13 77000667 frameshift variant AT/- delins 2
rs1057516390 1.000 0.120 13 76995901 splice acceptor variant G/- del 1
rs1057516814 1.000 0.120 13 76992171 frameshift variant TC/G delins 1
rs1057517134 1.000 0.120 13 76992250 frameshift variant ACTGGCCGGTGCC/- delins 1
rs121908292 1.000 0.120 13 77000799 stop gained G/T snv 1
rs147065248 1.000 0.120 13 76996034 missense variant T/C snv 1.2E-05 7.0E-06 1
rs1555273609 1.000 0.120 13 76992215 frameshift variant G/- delins 1
rs1555273882 1.000 0.120 13 76995079 frameshift variant C/- delins 1
rs1555273992 1.000 0.120 13 76995998 frameshift variant T/- delins 1
rs1555274014 1.000 0.120 13 76996128 splice donor variant G/A snv 1
rs1555274337 1.000 0.120 13 77000556 frameshift variant -/CAGAGACA delins 1
rs1555274344 1.000 0.120 13 77000605 frameshift variant CCTTTAAC/- del 1