Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
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
rs77191406 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs3219175 0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02 10
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26