Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1805127 0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs45546039 0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 15
rs766265889 0.827 0.240 2 178535508 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs120074192 0.763 0.120 11 2527959 missense variant A/G snv 10
rs7626962 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs3766871 0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 9
rs104894503 0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05 9
rs794728708 0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs104894580 0.790 0.240 17 70175238 missense variant C/A;T snv 4.0E-06 7
rs199473605 0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 7
rs56984562 0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs137854600 0.807 0.120 3 38551504 missense variant C/A;T snv 6
rs1860561 0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs104894584 0.851 0.120 17 70175553 missense variant G/A snv 5
rs121918600 0.882 0.080 1 237791441 missense variant C/T snv 5
rs59301204 0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 4
rs755373114 0.925 0.080 4 113341742 missense variant A/C snv 7.2E-05 3
rs192749597 0.882 0.080 12 2679712 missense variant C/T snv 9.2E-04 3.5E-03 3
rs1805120 0.882 0.080 7 150952443 synonymous variant G/A snv 0.30 0.26 3
rs120074187 0.882 0.120 11 2572963 missense variant G/A snv 4.8E-05 2.1E-05 3
rs761056344 0.925 0.080 6 118558994 missense variant C/G;T snv 4.0E-06; 3.2E-05 3