Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
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
rs989902 0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2839698 0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25
rs175080 0.776 0.240 14 75047125 missense variant G/A snv 0.40 0.43 9
rs1052748 0.925 0.080 17 4817174 missense variant C/T snv 0.39 0.36 2
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
rs2854746 0.752 0.200 7 45921046 missense variant G/A;C;T snv 0.38 14
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
rs203462 0.807 0.200 17 19909228 missense variant T/C snv 0.37 0.43 7
rs1065411 0.925 0.080 1 109690516 missense variant G/A;C;T snv 0.36; 6.9E-06 2
rs1801368 0.851 0.160 7 1936821 missense variant C/G;T snv 0.35 0.29 4
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
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