| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1060499900 | 0.925 | 0.080 | 3 | 38551304 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs137854602 | 0.925 | 0.080 | 3 | 38555664 | missense variant | G/A | snv | 5.6E-05 | 1.4E-05 | 1 | |
| rs137854603 | 1.000 | 0.080 | 3 | 38550602 | missense variant | C/T | snv | 6.0E-05 | 2.8E-05 | 1 | |
| rs137854604 | 0.882 | 0.120 | 3 | 38551243 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 1 | |
| rs137854615 | 0.851 | 0.120 | 3 | 38550989 | missense variant | A/G | snv | 1 | |||
| rs137854616 | 1.000 | 0.080 | 3 | 38566465 | missense variant | C/T | snv | 2.8E-05 | 7.0E-06 | 1 | |
| rs185492581 | 1.000 | 0.080 | 3 | 38630327 | stop gained | T/A;C | snv | 7.0E-06 | 1 | ||
| rs185638763 | 0.882 | 0.120 | 3 | 38599001 | missense variant | G/A;T | snv | 1.2E-05 | 1 | ||
| rs193922726 | 1.000 | 0.080 | 3 | 38551188 | missense variant | G/A;C | snv | 6.0E-05 | 1 | ||
| rs199473050 | 1.000 | 0.080 | 3 | 38633098 | missense variant | A/C | snv | 4.4E-05 | 1.4E-05 | 1 | |
| rs199473051 | 0.925 | 0.120 | 3 | 38633058 | missense variant | C/T | snv | 1 | |||
| rs199473052 | 1.000 | 0.080 | 3 | 38630425 | missense variant | A/G | snv | 1 | |||
| rs199473053 | 1.000 | 0.080 | 3 | 38630422 | missense variant | A/C | snv | 1 | |||
| rs199473054 | 1.000 | 0.080 | 3 | 38630420 | missense variant | C/G;T | snv | 2.0E-05; 2.8E-05 | 1 | ||
| rs199473056 | 1.000 | 0.080 | 3 | 38630376 | missense variant | G/A;T | snv | 3.6E-05; 4.0E-06 | 1 | ||
| rs199473058 | 0.925 | 0.080 | 3 | 38630341 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs199473061 | 1.000 | 0.080 | 3 | 38622446 | missense variant | C/T | snv | 1.2E-04 | 2.1E-05 | 1 | |
| rs199473063 | 1.000 | 0.080 | 3 | 38620929 | missense variant | C/G | snv | 1 | |||
| rs199473065 | 1.000 | 0.080 | 3 | 38620921 | missense variant | G/C | snv | 1 | |||
| rs199473066 | 1.000 | 0.080 | 3 | 38620910 | missense variant | A/G | snv | 1 | |||
| rs199473067 | 1.000 | 0.080 | 3 | 38620900 | missense variant | G/A;T | snv | 1.6E-05 | 1 | ||
| rs199473074 | 1.000 | 0.080 | 3 | 38613758 | missense variant | T/C | snv | 4.2E-06 | 1 | ||
| rs199473079 | 1.000 | 0.080 | 3 | 38609860 | missense variant | G/T | snv | 1 | |||
| rs199473081 | 1.000 | 0.080 | 3 | 38609841 | missense variant | A/T | snv | 1 | |||
| rs199473082 | 1.000 | 0.080 | 3 | 38609824 | missense variant | G/A;C | snv | 1 |