Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs772717932 1.000 0.040 2 112830530 missense variant C/A;T snv 4.0E-06; 1.6E-05 2
rs1143639 1.000 0.120 2 112831216 non coding transcript exon variant C/T snv 0.20 2
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs3788766 1.000 0.040 X 116435671 upstream gene variant G/A snv 2
rs1800076 0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 10
rs78655421 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs77932196 0.790 0.280 7 117540270 missense variant G/A;C;T snv 2.4E-05; 2.4E-05 8
rs74551128 0.807 0.160 7 117548795 missense variant C/A;T snv 5.3E-05; 5.7E-05 8
rs193922500 0.851 0.160 7 117548798 missense variant T/C snv 2.0E-04 4.9E-05 5
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs121908757 0.925 0.160 7 117587799 missense variant A/C snv 4.0E-06 3
rs121909005 0.851 0.160 7 117587801 missense variant T/A;C;G snv 4.0E-06; 8.0E-06 5
rs75527207 0.732 0.440 7 117587806 missense variant G/A snv 1.8E-04 3.0E-04 15
rs75541969 0.827 0.200 7 117614699 missense variant G/C snv 4.0E-04 3.2E-04 9
rs74767530 0.851 0.320 7 117627537 stop gained C/T snv 5.6E-05 4.9E-05 5
rs397508638 0.807 0.160 7 117652871 frameshift variant A/-;AA delins 9
rs80034486 0.807 0.160 7 117652877 missense variant C/G snv 1.4E-04 1.6E-04 9
rs113857788 0.882 0.160 7 117664780 missense variant G/C;T snv 1.0E-03; 6.0E-05 5
rs778055276 3 122555701 missense variant T/C snv 4.4E-05 3.5E-05 1
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs11575934 0.882 0.040 19 18075808 missense variant T/C snv 0.28 0.25 4