Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs965513 0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2145418 0.882 0.080 1 118422631 intergenic variant C/A snv 0.78 3
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
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
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs121913535 0.742 0.320 12 25245348 missense variant C/A;G;T snv 14
rs778212685 0.827 0.120 22 28712015 missense variant C/A;G;T snv 4.0E-06 8
rs768891111 0.851 0.080 14 103699474 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 4
rs538912281 0.925 0.080 9 97854657 missense variant C/A;G;T snv 2.0E-03 3
rs747463591 0.882 0.080 10 59906391 missense variant C/A;G;T snv 4.9E-06; 9.9E-06 3
rs78929565 0.882 0.080 4 55539035 intron variant C/A;T snv 3
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193