Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs28934906 0.716 0.320 X 154031355 missense variant G/A snv 46
rs397507520 0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs1400419650 0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 38
rs1555386022 0.708 0.320 14 92003418 splice donor variant C/A snv 38
rs387907144 0.716 0.600 6 157181056 stop gained C/A;T snv 34
rs113871094 0.683 0.320 15 48465820 stop gained G/A snv 34
rs1557781252 0.742 0.320 1 153816414 stop gained G/A snv 33
rs80338945 0.695 0.440 13 20189313 missense variant A/G snv 6.4E-04 6.4E-04 32
rs387907141 0.752 0.360 6 157181137 stop gained C/T snv 24
rs1558373252 0.790 0.120 2 5693013 frameshift variant T/- delins 19
rs397517154 0.763 0.280 2 39022773 missense variant C/A;G;T snv 4.0E-06 16
rs1554196416 0.851 0.200 6 78958551 stop gained G/A snv 15
rs1064797102 0.827 0.120 8 91071136 splice acceptor variant A/G snv 15
rs1555528356 0.790 0.360 16 89282836 stop gained G/A snv 13
rs1555649483 0.851 0.200 17 67909751 splice donor variant GAAGGACCAAGG/- del 12
rs876657380 0.851 0.360 6 157181155 frameshift variant AA/- delins 11
rs1057521737 0.827 0.240 22 41173768 missense variant T/C snv 11
rs1567263168 0.851 0.240 16 3729444 missense variant C/T snv 10
rs139073416 0.882 0.240 1 26795056 missense variant C/A;T snv 1.2E-04 9
rs886041239 1.000 0.160 10 110593202 missense variant A/G snv 9
rs879253745 0.925 0.240 6 157181040 frameshift variant AA/- delins 6
rs879253746 0.925 0.240 6 157200866 frameshift variant -/T delins 6
rs879253747 0.925 0.240 6 157167101 stop gained C/T snv 6
rs879253856 0.925 0.240 6 157110496 frameshift variant CCG/TCCGCAGCCACTCC delins 6