| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs529782627 | 0.882 | 0.120 | 21 | 26112051 | missense variant | C/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs553119528 | 0.882 | 0.160 | 17 | 44352489 | missense variant | G/A | snv | 5.2E-05 | 6.3E-05 | 3 | |
| rs63750151 | 0.882 | 0.080 | 21 | 25891761 | missense variant | C/G;T | snv | 3 | |||
| rs63751399 | 0.882 | 0.120 | 14 | 73171047 | missense variant | T/A;C | snv | 3 | |||
| rs6489630 | 0.882 | 0.080 | 12 | 5495458 | intron variant | T/C | snv | 0.75 | 3 | ||
| rs748703149 | 0.882 | 0.080 | 19 | 44908729 | missense variant | G/A;C;T | snv | 6.3E-06; 6.3E-06 | 3 | ||
| rs766647311 | 0.882 | 0.080 | 6 | 41159841 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
| rs767425642 | 0.882 | 0.120 | 17 | 63489010 | missense variant | G/A;T | snv | 3.2E-05; 4.0E-06 | 3 | ||
| rs8126696 | 0.882 | 0.080 | 21 | 37358422 | intron variant | T/C | snv | 0.64 | 3 | ||
| rs901115236 | 0.882 | 0.120 | 22 | 23767531 | missense variant | G/A;T | snv | 1.5E-05; 1.5E-05 | 3 | ||
| rs9397456 | 0.882 | 0.160 | 6 | 151926017 | intron variant | A/G;T | snv | 3 | |||
| rs950530102 | 0.882 | 0.160 | 6 | 56704357 | missense variant | C/T | snv | 3 | |||
| rs11931074 | 0.851 | 0.080 | 4 | 89718364 | intron variant | G/A;C;T | snv | 7 | |||
| rs63750802 | 0.851 | 0.080 | 14 | 73219144 | missense variant | T/G | snv | 7 | |||
| rs63751032 | 0.851 | 0.080 | 14 | 73219156 | missense variant | T/A;G | snv | 7 | |||
| rs11669576 | 0.851 | 0.160 | 19 | 11111624 | missense variant | G/A | snv | 4.3E-02 | 8.4E-02 | 6 | |
| rs185645212 | 0.851 | 0.240 | 15 | 89323504 | missense variant | C/A;T | snv | 8.0E-06; 9.7E-04 | 6 | ||
| rs1057518919 | 0.851 | 0.120 | 14 | 73171023 | missense variant | T/G | snv | 5 | |||
| rs201106962 | 0.851 | 0.080 | 4 | 89828156 | missense variant | A/C | snv | 8.0E-05 | 7.0E-05 | 5 | |
| rs223331 | 0.851 | 0.160 | 4 | 102872408 | intron variant | T/A;C | snv | 5 | |||
| rs63749835 | 0.851 | 0.080 | 14 | 73192799 | missense variant | T/C | snv | 5 | |||
| rs63750635 | 0.851 | 0.120 | 17 | 46014286 | missense variant | C/T | snv | 5 | |||
| rs1233347077 | 0.851 | 0.160 | 19 | 44905894 | missense variant | G/C | snv | 7.0E-06 | 4 | ||
| rs1801474 | 0.851 | 0.080 | 6 | 162201165 | missense variant | C/T | snv | 7.1E-02 | 5.3E-02 | 4 | |
| rs1997794 | 0.851 | 0.120 | 20 | 1994212 | 5 prime UTR variant | T/C | snv | 0.50 | 4 |