Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10506868 0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs11571378 0.925 0.080 12 950115 intron variant A/C;T snv 2
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs12241008 0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs6489769 0.851 0.120 12 963799 intron variant C/A;T snv 4
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7904519 0.763 0.240 10 113014168 intron variant A/G snv 0.55 9
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42