Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs2228014 0.752 0.240 2 136115514 synonymous variant G/A snv 4.6E-02 3.5E-02 14
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1051792 0.851 0.240 6 31411200 missense variant G/A snv 0.34 0.35 5
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31