Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199469465 0.672 0.560 16 30737343 stop gained C/A;T snv 50
rs1569509136 0.708 0.400 X 53647576 splice acceptor variant T/C snv 24
rs523349 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs1064795104 0.790 0.440 2 72498492 stop gained A/C snv 17
rs121909574 0.724 0.400 6 10404509 missense variant T/A;C;G snv 4.6E-06 17
rs1271572 0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs1057516030 0.807 0.280 21 37480785 stop gained -/A delins 14
rs1569309484 0.807 0.200 X 74591586 missense variant A/G snv 13
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv 11
rs1057518944 0.807 0.280 5 36984990 frameshift variant CT/- delins 9
rs1555706928 0.851 0.240 18 44951954 missense variant G/A snv 8
rs1110061 0.807 0.200 9 124500523 missense variant C/A;G snv 4.3E-06; 0.10 7
rs2066479 0.790 0.160 9 96235528 missense variant C/A;G;T snv 7.2E-02 7
rs132630297 0.925 0.280 X 134425256 stop gained C/A;T snv 6
rs1565286228 0.807 0.200 11 61766173 frameshift variant GCACCGGGCCCCCCATC/T delins 6
rs1037084691
WT1
0.827 0.160 11 32392031 missense variant C/G;T snv 5
rs1085307132 0.882 0.160 8 143817668 frameshift variant -/TTTT delins 5
rs1565308384 0.827 0.200 11 61784321 frameshift variant -/A delins 5
rs1057517779 0.851 0.160 9 124493083 missense variant G/A snv 4
rs121918508 0.851 0.360 10 121488035 missense variant C/T snv 4
rs765057534 0.851 0.240 15 51222402 missense variant C/T snv 4.0E-06 4
rs1020397 0.882 0.160 15 80426396 intron variant G/C;T snv 3
rs118192175 0.882 0.160 19 38494564 missense variant C/T snv 1.2E-05 3
rs371433324 0.882 0.120 13 36865689 missense variant C/A;T snv 4.0E-06; 1.2E-05 3
rs3757824 0.882 0.160 7 17296411 non coding transcript exon variant T/C;G snv 3