Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
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
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs3173615 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs537742207 1.000 0.080 7 76054974 missense variant A/G snv 8.0E-06 7.0E-06 3
rs1481950 1.000 0.080 8 53777725 intron variant C/A;G snv 2
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11
rs121909715
GSN
0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 8
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs267606900 1.000 10 30313926 missense variant T/C snv 1.4E-05 2
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs104894201 0.763 0.280 11 111908934 missense variant T/C snv 12
rs587777606 0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 6
rs759504704 0.882 0.200 11 78436786 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs34015634 0.851 0.120 12 40340380 missense variant T/C snv 3.2E-05 1.4E-05 8
rs35801418 0.827 0.120 12 40321114 missense variant A/G snv 7
rs407135 0.925 0.120 12 51017570 intron variant G/T snv 0.74 3
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs63750311 0.790 0.240 14 73192647 missense variant A/C snv 8