Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 24
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs174538 0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 21
rs11655237 0.724 0.280 17 72404025 non coding transcript exon variant C/T snv 0.16 17
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs3810366 0.732 0.280 19 45370684 5 prime UTR variant G/C;T snv 12
rs314276 0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs8173 0.763 0.240 20 56369735 3 prime UTR variant C/G;T snv 9
rs110419 0.827 0.200 11 8231306 intron variant A/G snv 0.42 8
rs8756 0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 7
rs2168101 0.827 0.200 11 8233861 intron variant C/A snv 0.24 7
rs11788747 0.851 0.240 9 36105267 synonymous variant A/C;G snv 4.0E-06; 0.34 6
rs1423753702
WT1
0.807 0.280 11 32396401 stop gained G/A snv 1.4E-05 6
rs11994014 0.827 0.200 8 24944767 intergenic variant A/G snv 0.70 5
rs12587 0.827 0.200 12 25205894 3 prime UTR variant T/G snv 0.49 5