| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs760687800 | 1.000 | 0.080 | 14 | 54411563 | missense variant | C/A;G | snv | 4.0E-06; 2.4E-05 | 1 | ||
| rs541820233 | 1.000 | 0.080 | 6 | 31119577 | intron variant | C/T | snv | 1 | |||
| rs12564469 | 1.000 | 0.080 | 1 | 6150910 | intron variant | G/A | snv | 0.41 | 1 | ||
| rs9434711 | 1.000 | 0.080 | 1 | 6151123 | missense variant | G/A;C | snv | 0.37; 4.0E-06 | 1 | ||
| rs515255 | 1.000 | 0.080 | 11 | 125627250 | intron variant | G/A | snv | 0.45 | 1 | ||
| rs3794186 | 1.000 | 0.080 | 11 | 68053569 | 3 prime UTR variant | G/A | snv | 8.4E-02 | 1 | ||
| rs6766361 | 1.000 | 0.080 | 3 | 151027254 | intron variant | C/A;G | snv | 1 | |||
| rs164207 | 1.000 | 0.080 | 3 | 32504199 | upstream gene variant | C/A | snv | 0.24 | 1 | ||
| rs3096380 | 1.000 | 0.080 | 16 | 71285743 | missense variant | G/A;C | snv | 0.94 | 1 | ||
| rs113155945 | 1.000 | 0.080 | 2 | 237378714 | missense variant | C/T | snv | 2.6E-02 | 1.1E-02 | 1 | |
| rs3809236 | 1.000 | 0.080 | 12 | 107093269 | 5 prime UTR variant | G/A;C | snv | 0.14 | 1 | ||
| rs1413975856 | 1.000 | 0.080 | 3 | 41224579 | missense variant | A/C | snv | 7.0E-06 | 1 | ||
| rs1553631896 | 1.000 | 0.080 | 3 | 41233836 | frameshift variant | -/A | delins | 1 | |||
| rs1305420126 | 1.000 | 0.080 | 4 | 106924184 | synonymous variant | G/A | snv | 8.0E-06 | 1 | ||
| rs3739298 | 1.000 | 0.080 | 8 | 13100516 | synonymous variant | C/A;T | snv | 0.37; 4.0E-06 | 1 | ||
| rs2295660 | 1.000 | 0.080 | 14 | 100734443 | synonymous variant | T/C | snv | 1.1E-02 | 1.2E-02 | 1 | |
| rs74723057 | 1.000 | 0.080 | 19 | 10818611 | intron variant | G/C | snv | 6.0E-02 | 1 | ||
| rs3218170 | 1.000 | 0.080 | 1 | 23521037 | missense variant | C/T | snv | 1 | |||
| rs8013403 | 1.000 | 0.080 | 14 | 89818395 | intron variant | A/G | snv | 0.27 | 1 | ||
| rs1336242054 | 1.000 | 0.080 | 4 | 109974747 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs157224 | 1.000 | 0.080 | 1 | 28886822 | upstream gene variant | C/A | snv | 9.3E-02 | 1 | ||
| rs1421 | 1.000 | 0.080 | 2 | 47386731 | 3 prime UTR variant | T/C | snv | 0.10 | 1 | ||
| rs6766459 | 1.000 | 0.080 | 3 | 135197201 | intron variant | G/T | snv | 0.69 | 1 | ||
| rs238417 | 1.000 | 0.080 | 19 | 45353210 | intron variant | G/C;T | snv | 0.59; 3.6E-05 | 1 | ||
| rs9383951 | 1.000 | 0.080 | 6 | 151974478 | intron variant | G/C | snv | 5.1E-02 | 1 |