| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6311 | 0.645 | 0.640 | 13 | 46897343 | upstream gene variant | C/T | snv | 0.40 | 41 | ||
| rs387906930 | 0.790 | 0.360 | 4 | 6301846 | missense variant | C/G;T | snv | 8 | |||
| rs4689388 | 0.882 | 0.360 | 4 | 6268329 | upstream gene variant | G/A | snv | 0.64 | 4 | ||
| rs199946797 | 0.882 | 0.360 | 4 | 6301467 | missense variant | C/A;T | snv | 6.7E-04 | 3 | ||
| rs71530910 | 0.882 | 0.360 | 4 | 6301680 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 3 | |
| rs145639028 | 0.925 | 0.320 | 4 | 6289047 | missense variant | G/A | snv | 2.2E-05 | 1.4E-05 | 2 | |
| rs797045076 | 1.000 | 0.320 | 4 | 6302441 | frameshift variant | TCTT/- | delins | 1.2E-04 | 1 | ||
| rs104893879 | 1.000 | 0.320 | 4 | 6301739 | stop gained | G/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs104893880 | 1.000 | 0.320 | 4 | 6291961 | stop gained | C/T | snv | 4.1E-06 | 1 | ||
| rs104893881 | 1.000 | 0.320 | 4 | 6302250 | stop gained | C/G;T | snv | 1 | |||
| rs13127445 | 1.000 | 0.320 | 4 | 6269423 | upstream gene variant | C/G | snv | 0.56 | 1 | ||
| rs1362648752 | 1.000 | 0.320 | 4 | 6289078 | frameshift variant | -/GGCCGTCGCGAGGCTG | delins | 4.4E-05 | 2.8E-05 | 1 | |
| rs1402999203 | 1.000 | 0.320 | 4 | 6301801 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs147974629 | 1.000 | 0.320 | 4 | 6301104 | missense variant | G/A;C;T | snv | 6.3E-04; 4.0E-06; 8.0E-06 | 1 | ||
| rs148953711 | 1.000 | 0.320 | 4 | 6291241 | missense variant | G/A | snv | 2.0E-05 | 4.9E-05 | 1 | |
| rs1560408865 | 1.000 | 0.320 | 4 | 6289109 | frameshift variant | C/- | delins | 1 | |||
| rs1801211 | 1.000 | 0.320 | 4 | 6301440 | missense variant | C/G;T | snv | 1 | |||
| rs199910987 | 1.000 | 0.320 | 4 | 6301405 | missense variant | G/A | snv | 1.0E-04; 4.0E-06 | 3.3E-04 | 1 | |
| rs28937890 | 1.000 | 0.320 | 4 | 6301966 | missense variant | C/T | snv | 3.2E-05 | 7.0E-05 | 1 | |
| rs28937891 | 1.000 | 0.320 | 4 | 6301879 | missense variant | G/A;T | snv | 4.8E-05; 8.0E-06 | 1 | ||
| rs28937892 | 1.000 | 0.320 | 4 | 6301306 | missense variant | C/A;T | snv | 4.0E-06; 3.6E-05 | 1 | ||
| rs35932623 | 1.000 | 0.320 | 4 | 6302247 | missense variant | C/T | snv | 5.0E-03 | 4.0E-03 | 1 | |
| rs369107336 | 1.000 | 0.320 | 4 | 6302164 | stop gained | C/A;G;T | snv | 3.3E-05; 1.9E-04 | 1 | ||
| rs369671890 | 1.000 | 0.320 | 4 | 6277628 | missense variant | C/A;T | snv | 2.3E-04 | 8.4E-05 | 1 | |
| rs372249044 | 1.000 | 0.320 | 4 | 6289068 | missense variant | G/A | snv | 1.4E-05 | 1.4E-05 | 1 |