Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs34778348 0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
rs35870237 0.763 0.120 12 40340404 missense variant T/C snv 9
rs34015634 0.851 0.120 12 40340380 missense variant T/C snv 3.2E-05 1.4E-05 8
rs34995376 0.807 0.080 12 40310435 missense variant G/A snv 7.0E-06 7
rs35801418 0.827 0.120 12 40321114 missense variant A/G snv 7
rs35507033 0.882 0.080 12 40313976 missense variant G/A;C snv 4.0E-03; 4.0E-06 3
rs111341148 0.925 0.040 12 40298346 missense variant G/A snv 3.2E-05 2.1E-05 2
rs17466213 0.925 0.040 12 40308618 missense variant A/G snv 8.6E-04 5.8E-04 2
rs281865054 0.925 0.040 12 40323270 stop gained G/A;T snv 4.0E-06 2
rs35173587 0.925 0.040 12 40284011 missense variant G/A;T snv 4.0E-06; 1.0E-03 2
rs35658131 0.925 0.040 12 40351723 missense variant A/G snv 3.5E-04 5.4E-04 2
rs74163686 0.925 0.040 12 40309225 missense variant A/C snv 2
rs78029637 1.000 12 40340436 missense variant A/T snv 7.0E-06 2
rs113511708 1.000 12 40363440 missense variant C/T snv 1.6E-04 2.4E-04 1
rs281865057 1.000 12 40367012 missense variant T/A snv 4.0E-06 1.4E-05 1
rs79546190 1.000 12 40363541 missense variant G/A snv 2.8E-05 2.8E-05 1
rs111691891 1.000 12 40351579 missense variant C/T snv 4.0E-06 4.9E-05 1
rs145364431 1.000 12 40322047 missense variant G/A;T snv 8.0E-06; 3.6E-05 1
rs199566791 1.000 12 40278154 missense variant A/G snv 1
rs201271001 1.000 12 40351585 missense variant G/A snv 5.2E-05 9.1E-05 1
rs281865045 1.000 12 40293644 missense variant A/G snv 1
rs281865052 1.000 12 40323255 missense variant A/G snv 1
rs33958906 1.000 12 40314059 missense variant C/T snv 3.2E-02 3.0E-02 1