Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs55832599 0.716 0.360 17 7673821 missense variant G/A snv 18
rs1225976306 0.807 0.160 7 140924673 missense variant C/T snv 9.3E-06 8
rs866419664 0.882 0.040 17 7673821 frameshift variant -/TCCCA delins 5
rs878854600 0.851 0.240 22 23834262 3 prime UTR variant C/T snv 4
rs387906812 0.882 0.320 22 23834152 missense variant G/A snv 7.0E-06 3
rs74315513 0.925 0.160 22 23787203 stop gained C/T snv 2
rs55945045 1.000 0.040 6 149701841 missense variant G/A snv 3.6E-03; 4.0E-06 3.4E-03 1
rs753300935
NF2
1.000 0.040 22 29661299 missense variant C/G;T snv 8.0E-06 7.0E-06 1