Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs5744533 0.807 0.120 5 75510279 intron variant C/A;T snv 6
rs7164773 0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs781172058 0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs786204929 0.752 0.200 10 87933144 stop gained G/A;T snv 12
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
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
rs766914563 0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs371074389 0.732 0.320 2 136115226 synonymous variant C/T snv 4.0E-06 4.2E-05 16
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs10506868 0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800067 0.716 0.320 16 13935176 missense variant G/A snv 5.6E-02 5.3E-02 17
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62