Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs78655421 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs75527207 0.732 0.440 7 117587806 missense variant G/A snv 1.8E-04 3.0E-04 15
rs17580 0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 14
rs721917 0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs1800076 0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 10
rs121917834 0.790 0.080 8 22163096 missense variant T/A;C snv 3.6E-05 10