Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28