Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs7439366 0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2306283 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs3803185 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs9904341 0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1056827 0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174