Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs12951053 0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs2293152 0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs16917546 0.851 0.040 10 62637778 intron variant T/C snv 0.29 6
rs2805831 1.000 0.040 9 97704354 intron variant G/A snv 0.18 2
rs79824801 1.000 0.040 12 56334353 intron variant T/C snv 4.5E-02 2
rs142310826 1.000 0.040 4 178481702 intergenic variant T/A snv 1.7E-02 3
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1356844630 0.925 0.160 12 57470802 stop gained C/T snv 4.0E-06 5
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
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1126809 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 29
rs1805007 0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25