Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137853313 1.000 0.080 X 154371130 missense variant G/C snv 1
rs137853315 0.882 0.200 X 154368081 missense variant G/A snv 1
rs1557180226 1.000 0.080 X 154371164 start lost T/C snv 1
rs1569551449 1.000 0.080 X 154352019 stop gained C/A snv 1
rs1569551736 1.000 0.080 X 154362043 frameshift variant C/- del 1
rs28935169 1.000 0.080 X 154371001 missense variant T/A snv 1
rs781910090 1.000 0.080 X 154351689 stop gained G/A;C snv 1.7E-05 1
rs782426283 1.000 0.080 X 154359317 missense variant G/A snv 3.6E-04 6.6E-05 1
rs80338841 1.000 0.080 X 154364625 synonymous variant G/A snv 1
rs863223295 1.000 0.080 X 154367639 splice donor variant A/G snv 1
rs863223296 1.000 0.080 X 154370872 splice donor variant C/T snv 1
rs863223297 1.000 0.080 X 154370955 frameshift variant GGCCG/- delins 1
rs863223299 1.000 0.080 X 154359402 frameshift variant C/- del 1