Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs2665390 0.776 0.160 3 156679960 intron variant C/T snv 0.92 8
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213