Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519440 1.000 0.040 X 51744647 missense variant G/A snv 3
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs113871094 0.683 0.320 15 48465820 stop gained G/A snv 34
rs113994098 0.742 0.320 15 89321792 missense variant C/T snv 1.5E-04 2.7E-04 10
rs28935468 0.732 0.240 X 154030912 missense variant G/A snv 14
rs587784105 0.732 0.440 5 177235863 stop gained G/A snv 19
rs61750240 0.752 0.240 X 154031020 stop gained G/A;C snv 5.5E-06 17
rs757511770 0.807 0.280 1 240092656 missense variant A/C;G;T snv 8.0E-06; 4.0E-06 9
rs768407867 0.925 0.160 2 174748177 missense variant C/T snv 4.4E-05 3.5E-05 3
rs794726827 0.827 0.120 2 166054637 splice donor variant C/A;G;T snv 6
rs80338945 0.695 0.440 13 20189313 missense variant A/G snv 6.4E-04 6.4E-04 32
rs876660634 0.807 0.200 10 87925551 missense variant A/C;G snv 10
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs1555565492 0.776 0.160 17 17795417 frameshift variant -/G delins 18
rs1555640521 0.790 0.320 18 6942110 frameshift variant A/- delins 15
rs1558373252 0.790 0.120 2 5693013 frameshift variant T/- delins 19
rs1566446604 0.882 0.080 14 21431511 frameshift variant GAGAGCTTGGCAGTCCA/- delins 6
rs1566823361 0.742 0.440 13 101726732 frameshift variant -/G delins 18
rs1568070621 1.000 0.040 17 67918746 frameshift variant AG/- delins 4
rs1569525894 0.790 0.280 X 136040055 frameshift variant TCTTCCTTAACCACCGC/- delins 14
rs558269137 0.851 0.160 1 152312601 frameshift variant ACTG/- delins 1.3E-02 8
rs1562127631 0.742 0.360 6 78961751 frameshift variant C/- del 24