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
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11547328 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs121913409 0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs1057519865 0.742 0.240 3 138946321 missense variant G/C snv 15
rs771138120 0.827 0.120 9 21971191 missense variant G/A;C;T snv 9.1E-06; 4.5E-06 13
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs1285136498 0.807 0.080 5 143400101 missense variant G/A snv 13
rs397507509 0.807 0.240 12 112450359 missense variant G/C;T snv 9
rs762292600 0.925 0.080 6 151944316 missense variant A/G snv 4.0E-06 1.4E-05 7
rs6674079 1 156516269 downstream gene variant A/G snv 0.34 3
rs886039463 1.000 0.080 12 112489096 missense variant C/A snv 3