Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607555 0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 6
rs267606879 0.925 0.080 14 104703428 missense variant G/A snv 7.0E-06 2
rs1283740147 1.000 0.080 19 45777777 missense variant C/T snv 4.0E-06 7.0E-06 1
rs121908415 0.925 0.080 19 38710286 missense variant A/G snv 7.0E-06 2
rs754313620 0.925 0.080 14 104714452 missense variant T/C;G snv 7.0E-06 2
rs761613959 0.851 0.080 1 155187356 stop gained G/A snv 3.2E-05 7.0E-06 4
rs779430565 0.882 0.080 11 101504316 missense variant T/A snv 1.2E-05 1.4E-05 3
rs140511594 0.742 0.360 2 165941111 missense variant G/A snv 1.3E-04 1.1E-04 13
rs119473033 0.827 0.320 2 216478216 stop gained G/T snv 8.0E-05 1.3E-04 11
rs149117087 1.000 0.080 2 227022069 missense variant T/A snv 8.5E-04 2.0E-04 1
rs74315342 0.763 0.120 1 179561327 missense variant C/T snv 6.0E-04 5.3E-04 10
rs2234591
WT1
0.925 0.080 11 32399873 intron variant T/C snv 1.4E-03 2
rs114896482 0.882 0.080 19 35842487 missense variant G/A snv 2.3E-03 1.5E-03 3
rs74315344 0.851 0.080 1 179575806 missense variant G/A snv 2.8E-03 4.2E-03 4
rs112545413 0.925 0.080 19 38717102 missense variant G/A snv 1.2E-02 9.6E-03 2
rs61747728 0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs3802829 0.925 0.080 11 101583461 missense variant G/A snv 8.2E-02 7.0E-02 2
rs4806213 1.000 0.080 19 35831699 missense variant T/C snv 9.7E-02 0.11 1
rs6508 0.882 0.160 11 32438918 non coding transcript exon variant G/A snv 8.3E-02 0.16 3
rs2071327 1.000 0.080 19 35831368 synonymous variant C/T snv 0.40 0.32 1
rs1799937
WT1
0.882 0.160 11 32389228 intron variant A/G snv 0.35 0.35 3
rs2301254 0.882 0.160 11 32436129 intron variant A/G snv 0.48 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2239785 0.827 0.240 22 36265284 missense variant G/A snv 0.79 0.68 5