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
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs225014 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs1805015 0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs143383 0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 17
rs143384 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17