| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs77716438 | 1.000 | 0.040 | 11 | 71216711 | intron variant | G/A | snv | 1.8E-02 | 1 | ||
| rs775988247 | 1.000 | 0.040 | 6 | 146399020 | missense variant | C/A;T | snv | 4.0E-06; 8.0E-06 | 1 | ||
| rs774917188 | 1.000 | 0.040 | 6 | 38677366 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs772572695 | 1.000 | 0.040 | 1 | 151406427 | missense variant | C/A;T | snv | 2.5E-05 | 1 | ||
| rs769581210 | 1.000 | 0.040 | 1 | 151405376 | missense variant | T/C | snv | 7.2E-05 | 3.5E-05 | 1 | |
| rs769402060 | 0.925 | 0.120 | 2 | 38075022 | missense variant | A/G | snv | 3.3E-05 | 4.2E-05 | 3 | |
| rs769236847 | 0.807 | 0.200 | 7 | 97869011 | missense variant | C/T | snv | 4.0E-06 | 3.5E-05 | 8 | |
| rs769224 | 1.000 | 0.040 | 22 | 19964281 | synonymous variant | G/A | snv | 3.0E-02 | 4.4E-02 | 1 | |
| rs768913131 | 0.925 | 0.040 | 2 | 50552821 | missense variant | G/A | snv | 3 | |||
| rs76717360 | 1.000 | 0.040 | 11 | 70525214 | intron variant | C/T | snv | 2.9E-03 | 1 | ||
| rs767058690 | 0.925 | 0.040 | 22 | 50720865 | missense variant | G/C;T | snv | 1.1E-03 | 2 | ||
| rs766483232 | 1.000 | 0.040 | 15 | 29114003 | missense variant | A/C;G | snv | 4.0E-06; 3.6E-04 | 1 | ||
| rs765619798 | 0.925 | 0.040 | 8 | 26864720 | missense variant | C/A;T | snv | 2 | |||
| rs763820362 | 1.000 | 0.040 | 1 | 151424045 | missense variant | C/T | snv | 2.4E-05 | 1 | ||
| rs7632287 | 1.000 | 0.040 | 3 | 8749760 | intron variant | G/A | snv | 0.32 | 2 | ||
| rs762735676 | 1.000 | 0.040 | 17 | 31221945 | frameshift variant | TTT/-;TTTT | delins | 6.6E-05 | 1 | ||
| rs762457833 | 1.000 | 0.040 | 3 | 12187389 | missense variant | G/C | snv | 9.8E-05 | 2.8E-05 | 1 | |
| rs762292772 | 0.882 | 0.160 | 22 | 50721505 | frameshift variant | G/-;GG | delins | 4 | |||
| rs76224556 | 1.000 | 0.040 | 22 | 50695096 | intron variant | C/A;T | snv | 2.0E-02 | 1 | ||
| rs762079123 | 1.000 | 0.040 | 8 | 1771125 | missense variant | G/A | snv | 2.0E-05 | 1 | ||
| rs7608798 | 0.925 | 0.040 | 2 | 162033707 | intron variant | G/A | snv | 0.35 | 2 | ||
| rs760211123 | 1.000 | 0.040 | 1 | 151405662 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs760059077 | 1.000 | 0.040 | 1 | 151405919 | missense variant | C/T | snv | 2.4E-05 | 2.1E-05 | 1 | |
| rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
| rs758352860 | 1.000 | 0.040 | 2 | 50531232 | missense variant | T/C | snv | 8.1E-06 | 1 |