Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41274221 0.851 0.160 7 100093577 mature miRNA variant C/T snv 6.4E-05 4.9E-05 6
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs1799768 0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs773829498 0.882 0.080 7 101130457 missense variant A/G snv 4.0E-06 3
rs4648068 0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs497116 0.925 0.080 11 104892390 stop lost A/G snv 4.3E-02 2
rs9770242 0.851 0.240 7 106285885 5 prime UTR variant C/A snv 0.79 5
rs61330082 0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs510432 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs506027 0.925 0.080 6 106326589 upstream gene variant G/A snv 0.57 2
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs58764888 1.000 0.080 3 11176005 intron variant T/A snv 5.8E-02 1
rs1143643 0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs17602729 0.925 0.080 1 114693436 stop gained G/A;T snv 8.6E-02 2
rs11216153 0.925 0.080 11 116834384 upstream gene variant G/T snv 0.16 2
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs368287711 0.851 0.120 11 117989554 missense variant C/A;T snv 2.0E-05; 2.4E-05 4
rs1419560997 0.925 0.080 11 117993410 splice region variant G/A snv 8.0E-06 7.0E-06 2
rs41279766 0.925 0.080 2 118970217 missense variant C/G;T snv 2.1E-03 2
rs2715267 0.925 0.080 3 122052011 upstream gene variant G/A;T snv 2