Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72554655 1.000 0.160 X 78040695 missense variant G/A snv 1
rs72554657 1.000 0.160 X 78042687 missense variant G/A snv 1
rs794729231 1.000 0.160 X 78011448 splice acceptor variant G/A;C snv 1
rs797045325 1.000 0.160 X 77989628 stop gained G/T snv 1
rs797045330 1.000 0.160 X 77998601 stop gained C/A snv 1
rs797045331 1.000 0.160 X 78003072 splice acceptor variant G/A snv 1
rs797045336 1.000 0.160 X 78009176 stop gained C/G snv 1
rs797045337 1.000 0.160 X 78009225 stop gained G/T snv 1
rs797045338 1.000 0.160 X 78011175 splice acceptor variant G/C snv 1
rs797045339 1.000 0.160 X 78011180 stop gained T/G snv 1
rs797045340 1.000 0.160 X 78011253 splice donor variant G/C snv 1
rs797045341 1.000 0.160 X 78011257 splice region variant G/A snv 1
rs797045342 1.000 0.160 X 78011452 stop gained G/A snv 1
rs797045344 1.000 0.160 X 78011498 missense variant G/A;C snv 1
rs797045346 1.000 0.160 X 78011662 stop gained T/A snv 1
rs797045347 1.000 0.160 X 78011679 splice region variant G/C snv 1
rs797045348 1.000 0.160 X 78011674 missense variant G/T snv 1
rs797045349 1.000 0.160 X 78012877 splice acceptor variant A/G snv 1
rs797045350 1.000 0.160 X 78012889 missense variant G/A snv 1
rs797045351 1.000 0.160 X 78012893 stop gained G/A snv 1
rs797045354 1.000 0.160 X 78013063 missense variant T/G snv 1
rs797045357 1.000 0.160 X 78014755 splice donor variant T/A snv 1
rs797045359 1.000 0.160 X 78015753 splice acceptor variant G/A snv 1
rs797045360 1.000 0.160 X 78015810 missense variant C/T snv 1
rs797045362 1.000 0.160 X 78020367 missense variant T/A snv 1