Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 25
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs2293607 0.807 0.200 3 169764547 non coding transcript exon variant T/A;C snv 6
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs786204929 0.752 0.200 10 87933144 stop gained G/A;T snv 12
rs7977932 0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
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
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107