Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1130866 0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs721917 0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1078761 1.000 0.120 20 33288875 missense variant A/C;G snv 4.1E-06; 0.30 2
rs11575934 0.882 0.040 19 18075808 missense variant T/C snv 0.28 0.25 4
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs1965708 0.851 0.200 10 79557289 missense variant G/T snv 0.22 0.25 6
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs35169799 0.925 0.200 11 64263769 missense variant C/T snv 4.9E-02 4.5E-02 5
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs17580 0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 14
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs1800076 0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 10
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs78655421 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs113857788 0.882 0.160 7 117664780 missense variant G/C;T snv 1.0E-03; 6.0E-05 5
rs75541969 0.827 0.200 7 117614699 missense variant G/C snv 4.0E-04 3.2E-04 9