Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057516265
CHM
1.000 0.080 X 86047532 start lost T/C snv 1
rs132630263
CHM
1.000 0.080 X 85900700 stop gained GG/TC mnv 1
rs132630264
CHM
1.000 0.080 X 85894214 stop gained G/T snv 1
rs132630265
CHM
1.000 0.080 X 85894227 stop gained C/A snv 1
rs132630266
CHM
1.000 0.080 X 85957918 stop gained G/A snv 1
rs132630267
CHM
1.000 0.080 X 85894201 stop gained G/T snv 1
rs1555958073
CHM
1.000 0.080 X 85978801 frameshift variant T/- delins 1
rs1556307713
CHM
1.000 0.080 X 85957977 splice acceptor variant T/C snv 1
rs386833676
CHM
1.000 0.080 X 85878962 splice donor variant -/A delins 1.2E-05 1
rs397514603
CHM
1.000 0.080 X 85879054 missense variant T/C snv 1
rs527236048
CHM
1.000 0.080 X 85958872 stop gained G/A snv 1
rs587776746
CHM
1.000 0.080 X 85878987 frameshift variant ACAA/- delins 9.5E-06 1
rs776256380
CHM
1.000 0.080 X 85958965 stop gained G/A snv 1
rs786204761
CHM
1.000 0.080 X 86027490 splice donor variant C/A;T snv 1
rs886041179
CHM
1.000 0.080 X 85958881 stop gained G/A snv 1