Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894060 0.882 0.120 8 1780316 missense variant C/T snv 3.2E-05 7.0E-06 3
rs104894064 0.882 0.120 8 1771124 missense variant C/G;T snv 1.0E-04; 2.4E-05 3
rs1057516582 1.000 0.120 8 1771317 frameshift variant A/- del 1
rs1057516867 1.000 0.120 8 1771101 frameshift variant T/- del 1
rs137852883 1.000 0.120 8 1771142 missense variant G/A;C;T snv 4.0E-06; 2.4E-05 1
rs139003032 1.000 0.120 8 1780512 missense variant A/G;T snv 2.0E-05; 3.3E-04 1
rs142269885 1.000 0.120 8 1771428 missense variant A/C;G;T snv 9.7E-04 1
rs143730802 0.882 0.160 8 1771055 start lost A/G snv 1.2E-05 7.0E-06 4
rs144495588 0.925 0.120 8 1771553 stop gained G/C;T snv 8.0E-06; 1.2E-05 2
rs149308952 1.000 0.120 8 1771524 missense variant A/G snv 1.6E-05 2.8E-05 1
rs1554448874 1.000 0.120 8 1771056 start lost T/C snv 1
rs1554448924 1.000 0.120 8 1771104 frameshift variant A/- del 1
rs1554449028 1.000 0.120 8 1771257 frameshift variant C/- delins 1
rs1554449047 1.000 0.120 8 1771280 stop gained C/T snv 1
rs1554449124 1.000 0.120 8 1771360 stop gained G/A snv 1
rs1554449136 1.000 0.120 8 1771366 stop gained G/A snv 1
rs1554451484 1.000 0.120 8 1780248 splice acceptor variant A/G snv 1
rs1554451504 1.000 0.120 8 1780299 frameshift variant T/- delins 1
rs188259026 1.000 0.120 8 1771563 missense variant C/G;T snv 4.0E-06; 1.2E-05 1
rs28940569 1.000 0.120 8 1780495 missense variant G/C snv 1
rs34238807 1.000 0.120 8 1771116 frameshift variant G/-;GG delins 4.0E-06 1
rs386834123 1.000 0.120 8 1771233 inframe deletion AAG/- delins 1
rs386834124 0.925 0.120 8 1771263 missense variant G/A snv 2.8E-05 1.4E-05 4
rs386834125 1.000 0.120 8 1771281 missense variant A/G snv 1
rs386834126 1.000 0.120 8 1771374 missense variant T/G snv 1