Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs574202455 1.000 0.120 5 87353228 missense variant C/T snv 1
rs201294938 1.000 0.120 14 30884617 missense variant A/G snv 8.0E-06 7.0E-06 1
rs754786373 1.000 0.120 15 51471365 missense variant C/T snv 3.6E-05 2.8E-05 1
rs117685390 1.000 0.120 13 20193170 upstream gene variant A/G snv 0.16 1
rs749431664 1.000 0.120 1 34785282 missense variant G/A;C snv 4.0E-06; 4.0E-06 1
rs1566538321 1.000 0.120 13 20222994 frameshift variant G/- delins 1
rs772862268 1.000 0.120 13 20223159 stop gained G/A snv 1.2E-05 2.8E-05 1
rs370564476 1.000 0.120 17 19024372 missense variant T/A snv 4.0E-06 1.4E-05 1
rs765136820 1.000 0.120 3 122001823 missense variant C/G snv 1.1E-04 2.8E-05 1
rs1465957812 1.000 0.120 10 77084649 missense variant G/A snv 1
rs76737438 1.000 0.120 11 2570686 missense variant G/C snv 1
rs144964568 1.000 0.120 1 34785465 stop gained C/T snv 2.0E-05 1.4E-05 1
rs778568636 1.000 0.120 18 46505856 missense variant C/A snv 6.4E-06 1
rs756215789 1.000 0.120 11 118263084 missense variant T/C snv 4.0E-06 1
rs371465450 1.000 0.120 12 80255183 stop gained C/T snv 4.5E-05 7.0E-05 1
rs757774496 1.000 0.120 12 80279038 stop gained C/A;T snv 3.4E-05 4.2E-05 1
rs1321703512 1.000 0.120 5 102477684 missense variant A/G snv 1.2E-05 1
rs750584965 1.000 0.120 3 46709171 missense variant G/A snv 2.0E-05 1.4E-05 1
rs5756795 1.000 0.120 22 37726115 missense variant T/C snv 0.39 0.35 1
rs56002719 1.000 0.120 4 6302122 missense variant A/T snv 3.8E-03 3.5E-03 1
rs71524353 1.000 0.120 4 6300948 stop gained G/A;T snv 1.2E-03 1
rs144446375 1.000 0.120 15 80881079 missense variant G/A snv 1.2E-05 4.2E-05 2
rs996035812 1.000 0.120 15 80925682 missense variant C/T snv 4.0E-06 7.0E-06 2
rs606231410 0.925 0.120 6 33189443 missense variant C/A;T snv 4.1E-06 2
rs794729665 0.925 0.120 6 24178385 missense variant T/G snv 2